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Article

Copy number variation at 6q13 functions as a long-range regulator and is associated with pancreatic cancer risk.

Carcinogenesis - 1 Jan 2012

Huang Liming, Yu Dianke, Wu Chen, Zhai Kan, Jiang Guoliang, Cao Guangwen, Wang Chunyou, Liu Yu, Sun Menghong, Li Zhaoshen, Tan Wen, Lin Dongxin

Abstract excerpt

Copy number variations (CNVs) have been recognized to contribute to phenotypic variations and to be associated with susceptibility to certain complex diseases. This study examined the functional significance of CNVR2966.1 at 6q13 and its association with pancreatic cancer susceptibility. The CNVR2966.1 was found to be a 10,379 bp nucleotides deletion/insertion within the uniform boundaries chromosome 6:...

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Share to Chromosomes, Human, Pair 6

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 22016467
DOI: 10.1093/carcin/bgr228

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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