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

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.Known and novel variant counts at a read-depth of ≥100 that overlapped genes and their flanking regions.变异位点若被收录于dbSNP数据库，则判定为已知变异。仅在两个样本中特有的变异的数量也已列出。各变异类型（依次为单核苷酸变异（SNV）、插入、缺失及替换）在对应样本中检测到的最低频率分别为：肿瘤样本中0.88%、3.7%、10.07%与4.57%，淋巴结样本中7.41%、3.01%、10.07%与2.78%。此外还统计了测序深度≥100、且与基因及其侧翼区域重叠的已知变异与新发变异的数量。