Author Correction: Patterns of somatic structural variation in human cancer genomes

Integration of genomics and transcriptomics highlights the crucial role of chromosome 5 open reading frame 34 in various human malignancies

“…Human malignancies are characterized by chromosome CNVs, which include genes that are in hundreds or thousands [3,17]. According to a growing amount of evidence, CNVs are recurring in several cancer types, with some of them having a probability of appearing in the early tumorigenesis stages, demonstrating that some cancer-associated CNVs may serve as human cancers drivers [30,31]. CNAs can speed up tumor growth by changing the gene expression levels whose location is at regions of the impacted genomic [32].…”