Test Code CMACB Chromosomal Microarray, Congenital, Blood
Specimen Type
Whole bloodOrdering Guidance
This test is not appropriate for detecting acquired copy number changes and excessive homozygosity. If this test is ordered with a reason for testing indicating a hematological disorder, the test will be canceled and CMAH / Chromosomal Microarray, Hematologic Disorders, Varies will be added and performed as the appropriate test.
Shipping Instructions
Advise Express Mail or equivalent if not on courier service.
Necessary Information
The reason for testing is required.
Specimen Required
This test requires 2 blood specimens: 1 sodium heparin and 1 EDTA.
Submit only 1 of the following specimen types:
Specimen Type: Whole blood
Container/Tube: Green top (sodium heparin) and lavender top (EDTA)
Specimen Volume: 3-mL EDTA tube and 4-mL sodium heparin tube
Collection Instructions:
1. Invert several times to mix blood.
2. Send whole blood specimens in original tubes. Do not aliquot.
Specimen Type: Cord blood
Container/Tube: Green top (sodium heparin) and lavender top (EDTA)
Specimen Volume: 3-mL EDTA tube and 4-mL sodium heparin tube
Note: The lab will attempt testing on a minimum of 1-mL whole blood, EDTA preferred.
Collection Instructions:
1. Invert several times to mix blood.
2. Send cord blood specimens in original tubes. Do not aliquot.
3. Label specimen as cord blood.
Specimen Minimum Volume
2 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Whole blood | Ambient (preferred) | ||
Refrigerated |
Reject Due To
All specimens will be evaluated at Mayo Clinic Laboratories for test suitability.Reference Values
An interpretive report will be provided.
Day(s) Performed
Monday through Sunday
Report Available
7 to 14 daysSpecimen Retention Time
Four weeksPerforming Laboratory
Mayo Clinic Laboratories in RochesterCPT Code Information
81229