Gene copy number variation and common human disease

M Fanciulli, E Petretto, T J Aitman

Research output: Contribution to journalArticlepeer-review


Variation in gene copy number is increasingly recognized as a common, heritable source of inter-individual differences in genomic sequence. The role of copy number variation is well established in the pathogenesis of rare genomic disorders. More recently, germline and somatic copy number variation have been shown to be important pathogenic factors in a range of common diseases, including infectious, autoimmune and neuropsychiatric diseases and cancer. In this review, we describe the range of methods available for measuring copy number variants (CNVs) in individuals and populations, including the limitations of presently available assays, and highlight some key examples of common diseases in which CNVs have been shown clearly to have a pathogenic role. Although there has been major progress in this field in the last 5 years, understanding the full contribution of CNVs to the genetic basis of common diseases will require further studies, with more accurate CNV assays and larger cohorts than have presently been completed.

Original languageEnglish
Pages (from-to)201-13
Number of pages13
JournalClinical genetics
Issue number3
Publication statusPublished - Mar 2010


  • Animals
  • Disease
  • Gene Dosage
  • Genetic Predisposition to Disease
  • Humans
  • Molecular Biology


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