Fig. 4

Genomic landscape of CNVs and gene fusions in NSCLC patients. A Oncoprint diagram showing the distribution of copy number variations (CNVs) in the NSCLC patient cohort. The X-axis represents individual patient samples, while the Y-axis lists the affected genes. Red indicates gene amplifications, and gray denotes no alterations. B Distribution of gene fusions in the NSCLC patient cohort. The X-axis represents individual patient samples, and the Y-axis shows the fusion variants. Purple represents structural variants, pink denotes exon skipping, and gray indicates no alterations