Special Instructions

Test orders must include an attestation that the provider has the patient's informed consent for genetic testing. In cases where a known mutation is documented, the physician may prefer to order test 252727. For family tests, submit the result report of the first patient tested if not performed at a LabCorp facility.

Limitations

The method does not reliably detect mosaic variants, large deletions, duplications, inversions, or other rearrangements, and deep intronic variants. It may be affected by allele-dropout and does not determine the exact numbers of T/A or microsatellite repeats. It also cannot conclude if two heterozygous variants are on the same chromosome copy. This test was developed by Labcorp and has not been FDA cleared or approved.

Biomarkers

Result Turnaround Time

Related Documents