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. Author manuscript; available in PMC: 2020 Aug 11.
Published in final edited form as: Cell. 2019 Oct 31;179(4):964–983.e31. doi: 10.1016/j.cell.2019.10.007

Figure 1. Genomic Alterations and their Associations with mRNA, Protein, and Phosphoprotein Abundances.

Figure 1.

(A) Profiling of absolute copy number estimates observed in the CPTAC cohort. Genomically defined non-ccRCC tumors are above ccRCC tumors; translocation event, grade, CpG island methylator phenotype (CIMP) status, genome instability, and CNV loss/gain are indicated by color coding. ccRCC tumors with evidence of 3p loss of heterozygosity (LOH) are indicated by three asterisks (***).

(B) Circos plots of translocation events involving chromosomes 3 and either chromosomes 5 (red), 2 (blue), 8 (purple) or all other chromosomes (gray), including chromosomal inversion within chromosome 3 (green). Percentage of involved tumors with re-arrangement for each chromosome is annotated below each plot.

(C) Heatmap of multi-omic data for the five key tumor suppressor genes (VHL, PBRM1, BAP1, SETD2, and KDM5C) (n = 103). Tumor samples were ordered by 3p CNV alteration (loss to neutral). Non-ccRCC tumors are separated (right). CNV event, Z score, CNV loss/gain, translocation status, CpG island methylator phenotype (CIMP) status, genome instability, grade, and gender are indicated by color coding (bottom).

See also Figure S1 and Tables S1 and S2.