Full sequencing of the BRCA1/2 genes, plus deletion/duplication analysis. May be used to assess the risk of carrying a BRCA1/2 mutation when there is no known familial mutation.
Targeted analysis of the founder mutations found within the Ashkenazi Jewish population. May be used as a first line test for individuals of Ashkenazi Jewish descent, if negative the option to run a Comprehensive BRCA1/2 Analysis is available.
Targeted sequencing for specific familial or known mutations on the BRCA1 gene.
Targeted sequencing for specific familial or known mutations on the BRCA2 gene.
May be used to detect the presence of a deletion or duplication in the BRCA1/2 genes after previous sequencing tests were negative and deletion/duplication analysis was not offered.