Supplementary Tables S1-S12 from Whole-Genome Sequencing of Common Salivary Gland Carcinomas: Subtype-Restricted and Shared Genetic Alterations

Table S1. Detail clinical characteristics of the cohort. Table S2. Clinicopathologic Characteristics of the Cohort Across Salivary Gland Carcinoma Subtypes. Table S3. Summary statistics of the sequenced salivary gland carcinoma subtypes. Talbe S4. Summary statistics of the whole genome sequencing for each sample. Table S5. Number of different somatic alterations found in each tumor. Table S6. Genes effected by putative somatic MEI events. Table S7. Somatic copy number variations (CNVs) in each tumors. Table S8. Incidence of somatic copy number variations of known cancer driver genes in each tumors. Table S9. Rearrangements leading to potential fusion events. Table S10. Somatic mutations identified in each tumor. Table S11. Putative germline variations associated with the salivary cancer development*. Table S12. Difference among subtypes in abundances of molecular factors used in univariate statistical models.