Test Code WAGDR Alpha Globin Cluster Locus Deletion/Duplication, Blood
Ordering Guidance
Sequence variants, other than the alpha T-Saudi and hemoglobin Constant Spring alterations, are not detected by this assay. For detection of single point and other nondeletion variants, order WASEQ / Alpha Globin Gene Sequencing, Varies, if clinically indicated.
Shipping Instructions
Specimen Required
Patient Preparation: A previous bone marrow transplant from an allogeneic donor will interfere with testing. For instructions for testing patients who have received a bone marrow transplant, call 800-533-1710.
Specimen Type: Whole blood
Container/Tube:
Preferred: Lavender top (EDTA)
Acceptable: Yellow top (ACD)
Specimen Volume: 3 mL
Collection Instructions:
1. Invert several times to mix blood.
2. Send whole blood specimen in original tube. Do not aliquot.
Forms
1. 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 in Special Instructions:
-Informed Consent for Genetic Testing (T576)
-Informed Consent for Genetic Testing-Spanish (T826)
2. Molecular Genetics: Congenital Inherited Diseases Patient Information (T521)
Useful For
Diagnosis of alpha-thalassemia
Carrier screening for individuals from high-risk populations for alpha-thalassemia
This test is not useful for diagnosis or confirmation of beta-thalassemia or hemoglobinopathies.
Special Instructions
Method Name
Dosage Analysis by Polymerase Chain Reaction (PCR)/Quantitative Polymerase Chain Reaction (qPCR)/Multiplex Ligation-Dependent Probe Amplification (MLPA)
Reporting Name
Alpha Globin Clustr Locus Del/Dup,BSpecimen Type
VariesSpecimen Minimum Volume
Blood: 1 mL
Specimen Stability Information
Specimen Type | Temperature | Time |
---|---|---|
Varies | Varies |
Reference Values
An interpretive report will be provided.
Interpretation
The interpretive report includes an overview of the findings as well as the associated clinical significance.
Clinical Reference
1. Harteveld CL, Voskamp A, Phylipsen M, et al. Nine unknown rearrangements in 16p13.3 and 11p15.4 causing alpha- and beta-thalassaemia characterized by high resolution multiplex ligation-dependent probe amplification. J Med Genet. 2005;42(12):922-931. doi:10.1136/jmg.2005.033597
2. Harteveld CL, Higgs DR. Alpha-thalassemia. Orphanet J Rare Dis. 2010;5:13. doi:10.1186/1750-1172-5-13
3. Bunn HF, Forget BG. Hemoglobin: Molecular, Genetic and Clinical Aspects. 2nd ed. WB Saunders Company; 1986
4. Weatherall DJ, Higgs DR, Clegg JB, Hill AS, Nicholls R. Heterogeneity and origins of the alpha-thalassemias. Birth Defects Origi Artic Ser. 1987;23(5A):3-14
5. Musallam KM, Cappellini DM, Coates TD, et al. ?lpha-thalassemia: A practical overview. Blood Rev. 2024;64:101165. doi.10.1016/j.blre.2023.101165
Day(s) Performed
Varies
Report Available
9 to 13 daysPerforming Laboratory

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
81269
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
WAGDR | Alpha Globin Clustr Locus Del/Dup,B | 90040-7 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
621362 | Result Summary | 50397-9 |
621363 | Result | 82939-0 |
621364 | Interpretation | 69047-9 |
621365 | Additional Information | 48767-8 |
621366 | Specimen | 31208-2 |
621367 | Source | 31208-2 |
621368 | Method | 85069-3 |
621804 | Disclaimer | 62364-5 |
621369 | Released By | 18771-6 |