Copy number variants and genetic traits

Closer to the resolution of phenotypic to genotypic variability

Jacques S. Beckmann, Xavier P. Estivill, Stylianos E. Antonarakis

Research output: Contribution to journalReview article

294 Citations (Scopus)

Abstract

A considerable and unanticipated plasticity of the human genome, manifested as inter-individual copy number variation, has been discovered. These structural changes constitute a major source of inter-individual genetic variation that could explain variable penetrance of inherited (Mendelian and polygenic) diseases and variation in the phenotypic expression of aneuploidies and sporadic traits, and might represent a major factor in the aetiology of complex, multifactorial traits. For these reasons, an effort should be made to discover all common and rare copy number variants (CNVs) in the human population. This will also enable systematic exploration of both SNPs and CNVs in association studies to identify the genomic contributors to the common disorders and complex traits.

Original languageEnglish
Pages (from-to)639-646
Number of pages8
JournalNature Reviews Genetics
Volume8
Issue number8
DOIs
Publication statusPublished - 3 Aug 2007
Externally publishedYes

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Penetrance
Aneuploidy
Human Genome
Single Nucleotide Polymorphism
Population

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Genetics(clinical)

Cite this

Copy number variants and genetic traits : Closer to the resolution of phenotypic to genotypic variability. / Beckmann, Jacques S.; Estivill, Xavier P.; Antonarakis, Stylianos E.

In: Nature Reviews Genetics, Vol. 8, No. 8, 03.08.2007, p. 639-646.

Research output: Contribution to journalReview article

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