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HelpTest Code CHRCV Chromosome Analysis, Chorionic Villus Sampling
Useful For
Prenatal diagnosis of chromosome abnormalities, including aneuploidy (ie, trisomy or monosomy) and balanced rearrangements
This test is not appropriate as a first-tier test for detecting gains or losses of chromosomal material in pregnancies with 1 or more major structural abnormalities.
Reflex Tests
| Test ID | Reporting Name | Available Separately | Always Performed |
|---|---|---|---|
| _ML15 | Metaphases, <15 | No, (Bill Only) | No |
| _M15 | Metaphases, 15 | No, (Bill Only) | No |
| _MG14 | Metaphases, >15 | No, (Bill Only) | No |
| _KTG1 | Karyotypes, >1 | No, (Bill Only) | No |
| _STAC | Ag-Nor/CBL Stain | No, (Bill Only) | No |
Testing Algorithm
This test is not appropriate as a first-tier test for detecting gains or losses of chromosomal material in pregnancies with 1 or more major structural abnormalities.
This test includes a charge for cell culture of fresh specimens and professional interpretation of results. Analysis charges will be incurred for total work performed, and generally include 2 banded karyograms and the analysis of 20 metaphase cells. If no metaphase cells are available for analysis, no analysis charges will be incurred. If additional analysis work is required, additional charges may be incurred.
Special Instructions
Method Name
Cell Culture Followed by Chromosome Analysis
Reporting Name
Chromosomes, Chorionic Villus SampSpecimen Type
TissueOrdering Guidance
This test should be performed for prenatal diagnostic purposes only. A chromosomal microarray (CMAP / Chromosomal Microarray, Prenatal, Amniotic Fluid/Chorionic Villus Sampling) is recommended, rather than chromosomal analysis, to detect clinically relevant gains or losses of chromosomal material in pregnancies with 1 or more major structural abnormalities. Chromosomal microarray can also be considered, rather than chromosome analysis, for patients undergoing invasive prenatal diagnostic testing with a structurally normal fetus.
Portions of the specimen may be used for other tests such as molecular genetic testing, biochemical testing, and fluorescence in situ hybridization (FISH) testing (including PADF / Prenatal Aneuploidy Detection, FISH). If additional molecular genetic or biochemical genetic testing is needed, order CULFB / Fibroblast Culture for Genetic Test so that cell cultures may be set up specifically for the use in these tests.
Shipping Instructions
Advise Express Mail or equivalent if not on courier service.
Necessary Information
Provide a reason for referral with each specimen. The laboratory will not reject testing if this information is not provided, but appropriate testing and interpretation may be compromised or delayed.
Specimen Required
Specimen Type: Chorionic villi
Supplies: CVS Media (RPMI) and Small Dish (T095)
Container/Tube: 15-mL tube containing 15 mL of transport media
Specimen Volume: 20-30 mg
Collection Instructions:
1. Collect chorionic villus specimen (CVS) by the transabdominal or transcervical method.
2. Transfer the CVS to a Petri dish containing transport medium (Such as CVS Media [RPMI] and Small Dish [T095]).
3. Using a stereomicroscope and sterile forceps, assess the quality and quantity of the villi and remove any blood clots and maternal decidua.
4. If ordering with PADF / Prenatal Aneuploidy Detection, FISH, submit a minimum of 14 mg.
5. If ordering with CMAP / Chromosomal Microarray, Prenatal, Amniotic Fluid/Chorionic Villus Sampling, submit a minimum of 24 mg.
6. If ordering with both PADF and CMAP, then submit a minimum of 26 mg.
Specimen Minimum Volume
The following is the minimum volume when only this test is ordered:
12 mg
Specimen Stability Information
| Specimen Type | Temperature | Time | Special Container |
|---|---|---|---|
| Tissue | Refrigerated (preferred) | ||
| Ambient | |||
Reference Values
An interpretive report will be provided.
Interpretation
Cytogenetic studies on chorionic villus specimens (CVS) are considered nearly 100% accurate for the detection of non-mosaic whole chromosome abnormalities. Most sub-chromosomal abnormalities greater than 5-20Mb are also easily detectable dependent on size, location, and quality of the metaphase chromosomes. Very subtle or cryptic abnormalities involving microdeletions/duplication can typically only be detected by chromosomal microarray or targeted fluorescence in situ hybridization testing.
Approximately 3% of CVS samples analyzed are found to have chromosome abnormalities. Some of these chromosome abnormalities are balanced and may not be associated with birth defects. A normal karyotype does not rule out the possibility of birth defects, such as those caused by submicroscopic cytogenetic abnormalities, pathogenic molecular variants, and environmental factors (ie, teratogen exposure). For these reasons, clinicians should inform their patients of the technical limitations of chromosome analysis before the procedure is performed, so that patients may make an informed decision about pursuing the procedure.
Limitations:
-Abnormal results from CVS analysis may represent confined placental mosaicism and may not reflect the fetal karyotype.
-Only large abnormalities visible by manual inspection are detectable; subtle structural chromosome abnormalities may be missed
-Artifacts of cell culture may very rarely be misinterpreted as mosaicism in the sample.
It is recommended that a qualified professional in Medical Genetics communicate all results to the patient.
Clinical Reference
1. American College of Obstetricians and Gynecologists Committee on Genetics. Committee Opinion No. 581: the use of chromosomal microarray analysis in prenatal diagnosis. Obstet Gynecol. 2013;122:1374-1377
2. Society for Maternal-Fetal Medicine (SMFM). The use of chromosomal microarray for prenatal diagnosis. Am J Obstet Gynecol. 2016;215:B2-B9
3. Committee Opinion, 640. Cell-free DNA screening for fetal aneuploidy. American College of Obstetricians and Gynecologists Committee on Genetics. Obstet Gynecol. 2015;123:e31-e37
4. Wilson KL, Czerwinski JL, Hoskovec JM, et al. NSGC practice guideline: prenatal screening and diagnostic testing options for chromosome aneuploidy. J Genet Couns. 2013;22:4-15
Day(s) Performed
Monday through Friday
Report Available
9 to 14 daysPerforming Laboratory
Mayo Clinic Laboratories in Rochester
Test Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.CPT Code Information
88235, 88291-Tissue culture for amniotic fluid or chorionic villus cells, Interpretation and report
88267 w/modifier 52-Chromosome analysis, amniotic fluid or chorionic villus, <15 cells, 1 karyotype with banding (if appropriate)
88267-Chromosome analysis, amniotic fluid or chorionic villus, 15 cells, 1 karyotype with banding (if appropriate)
88267, 88285-Chromosome analysis, amniotic fluid or chorionic villus, <15 cells, 1 karyotype with banding (if appropriate)
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| CHRCV | Chromosomes, Chorionic Villus Samp | 62350-4 |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| 52319 | Result Summary | 50397-9 |
| 52321 | Interpretation | 69965-2 |
| 52320 | Result | 82939-0 |
| CG769 | Reason for Referral | 42349-1 |
| 52322 | Specimen | 31208-2 |
| 52323 | Source | 31208-2 |
| 52325 | Method | 85069-3 |
| 52324 | Banding Method | 62359-5 |
| 54624 | Additional Information | 48767-8 |
| 52326 | Released By | 18771-6 |
Forms
New York Clients-Informed consent is required. Document on the request form or electronic order that a copy is on file. The following documents are available: