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Human genetics

Sharp focus on the variable genome

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Copy-number variation — deleted or duplicated regions of DNA — is widespread in the human genome. A systematic population survey of the common variants provides an invaluable resource for further studies.

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Figure 1: Demonstrating copy-number variants (CNVs) related to disease.

References

  1. Conrad, D. F. et al. Nature doi:10.1038/nature08516 (2009). | Article

  2. Iafrate, A. J. et al. Nature Genet. 36, 949–951 (2004).

    Article  CAS  Google Scholar 

  3. Redon, R. et al. Nature 444, 444–454 (2006).

    Article  ADS  CAS  Google Scholar 

  4. Korbel, J. O. et al. Science 318, 420–426 (2007).

    Article  ADS  CAS  Google Scholar 

  5. Kidd, J. M. et al. Nature 453, 56–64 (2008).

    Article  ADS  CAS  Google Scholar 

  6. The Wellcome Trust Case Control Consortium Nature 447, 661–678 (2007).

  7. McCarroll, S. A. et al. Nature Genet. 40, 1107–1112 (2008).

    Article  CAS  Google Scholar 

  8. de Cid, R. et al. Nature Genet. 41, 211–215 (2009).

    Article  CAS  Google Scholar 

  9. Willer, C. J. et al. Nature Genet. 41, 25–34 (2009). | Article

    Article  CAS  Google Scholar 

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Armour, J. Sharp focus on the variable genome. Nature 461, 735–736 (2009). https://doi.org/10.1038/461735a

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