U.S. flag

An official website of the United States government

GTR Home > Tests > Aortopathy Panel, Sequencing and Deletion/Duplication

Performance Characteristics

Availability

Help

  • Entire test performed in-house

Analytical Validity

Help

The analytical sensitivity of this test is approximately 99% for single nucleotide variants (SNVs) and greater than 93% for insertions/duplications/deletions from 1-10 base pairs in size. Variants greater than 10 base pairs may be detected, but the analytical sensitivity may be reduced.

http://ltd.aruplab.com/Tests/Pdf/100

Proficiency Testing (PT)

Is proficiency testing performed for this test? Help
Yes
Method used for proficiency testingHelp
Intra-Laboratory

FDA Regulatory Clearances of the Test

Help

Not provided

New York State CLEP (NYS CLEP) Test Approval

Help
NYS CLEP test approval #
4196
Status
Approved

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.