Known and novel variant counts at a read-depth of ≥100 that overlapped genes and their flanking regions.

<p>Variants were judged as known by their being listed in dbSNP. Variant counts for those unique to both samples are also shown. The lowest frequency variant detected for each variant type (SNV, insertion, deletion, and substitution, respectively) in each sample was 0.88%, 3.7%, 10.07%, and 4.57% in the tumor, and 7.41%, 3.01%, 10.07%, 2.78% in the node.</p><p>Known and novel variant counts at a read-depth of ≥100 that overlapped genes and their flanking regions.