Supplementary Tables 1 - 9 from EGFR Variant Heterogeneity in Glioblastoma Resolved through Single-Nucleus Sequencing

XLSX file - 424KB, 9 tables containing segmented copy number, SCNAs, chromosomal rearrangements and whole-exomes sequencing data for BT325 and BT340. Table S1: EGFR alterations in TCGA samples with matching RNA and DNA sequencing. Table S2: Genes identified in the chromosome 6-9 amplicon in BT340. Table S3: BT325 segmented copy number data. Table S4: BT340 segmented copy number data. Table S5: BT340 copy number aberrations. Table S6: BT340 chromosomal rearrangements. Table S7: BT325 copy number aberrations and chromosomal rearrangements (each color denotes segments that are joined in one derivative chromosome). Table S8: Somatic SNVs and short insertion/deletions detected in BT325 from whole-exome sequencing data. Table S9: Somatic SNVs and short insertion/deletions detected in BT340 from whole-exome sequencing data.