Specifically, tumours from African individuals were more likely to have CNAs and mutations in SETBP1 (frequency = 0.33, odds ratio (OR) = 0.357, P = 0.012), DDX11L1 (frequency = 0.48, OR = 0.24, P = 0.0001), STK19 (frequency = 0.25, OR = 0.215, P = 0.004) and NCOA2 (frequency = 0.51, OR = 0.172, P = 3.14 × 10−6), along with SVs in PCAT1 (frequency = 0.13, OR = 0.11, P = 0.012). The gene discussed is PCAT1; the disease is neoplasm.