|
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z # |
Chromosomal Microarray, Postnatal Familial Follow-up, ClariSure® Oligo-SNP
Test Code39910
CPT Codes
81479
Preferred Specimen
5 mL whole blood collected in a sodium heparin (green-top) tube
Minimum Volume
3 mL whole blood
Other Acceptable Specimens
Whole blood collected in sodium heparin (royal blue-top), sodium heparin lead-free (tan-top) tube, or EDTA (lavender-top) tube • Buccal swab collected in ORAcollect Dx OCD-100/OCD-100A • 2 mL saliva collected in 0GD-500 Oragene Dx collection kit (up to the "fill to" line on device, do not count bubbles)
Instructions
Specimen viability decreases during transit. Send specimen to testing lab for viability determination. Do not freeze. Do not reject.
Transport Temperature
Room temperature
Specimen Stability
Room temperature: Preferred
Refrigerated: Acceptable
Frozen: Unacceptable
Refrigerated: Acceptable
Frozen: Unacceptable
Methodology
Oligo-SNP Array
FDA Status
This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by the U.S. Food and Drug Administration. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.
Setup Schedule
Monday-Sunday Morning
Report available: 10 Days
Report available: 10 Days
Reference Range
See Laboratory Report
Clinical Significance
To assist in establishing the clinical significance when a relative's chromosomal microarray study reveals a copy number variant. This test determines the familial presence or absence of a specific CNV identified by chromosomal microarray testing in a proband.