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. 2014 Oct 5;9(2):422–436. doi: 10.1016/j.molonc.2014.09.010

Table 3.

List of regions differentiating the clusters defined in HGSOCs.

Cytoband Start [bp] End [bp] Size [bp] Nr of genes Frequency in cluster A [%] Frequency in cluster B [%] Difference Cancer gene census P HR 95% CI P adj
6q24.2 – q26 145,593,087 162,867,181 17,274,094 169 14.29 75.55 61.26 0.001 0.06 0.01 0.43 0.005
11p15.5–15.3 0 12,467,187 12,467,187 393 9.56 67.65 58.09 HRAS CARS NUP98 LMO1 0.07 0.30 0.06 1.41 0.13
16q21 62,541,693 64,974,691 2,432,998 4 25.00 76.92 51.92 CDH11 0.71 0.62 0.15 2.60 0.51
19q13.31 – q13.32 48,908,403 51,085,851 2,177,448 73 1.56 51.92 50.36 BCL3 CBLC ERCC2 0.17 0.31 0.04 2.34 0.26
22q12.3 – q13.1 35,051,869 37,251,402 2,199,533 110 25.00 78.85 53.85 MYH9 0.56 0.25 0.04 1.56 0.14
22q13.2 – q13.31 39,940,439 46,673,931 6,733,492 105 26.25 80.77 54.52 0.72 0.53 0.08 3.30 0.49

Regions differentiating clusters (Clusters A and B) in the high‐grade serous ovarian carcinomas (HGSOCs) defined to be at least 35% more frequent in one of the clusters and significant after correction for multiple testing (FDR <0.05); all the regions were tested for the association with overall survival (OS), highlighted regions were significantly associated with better prognosis (P < 0.05), P‐values‐calculated in the univariate analysis with the log‐rank test; Padj as calculated in multivariate Cox regression model in which significant covariates were included; HR, Hazard Ratio; CI, Confidence Intervals.