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Pitfalls in the use of DGV for CNV interpretation

Aude Duclos1, Françoise Charbonnier, Pascal Chambon

  • 1Inserm U, Faculty of Medicine, Rouen University, France.

American Journal of Medical Genetics. Part A
|September 13, 2011
PubMed
Abstract

No abstract available in PubMed .

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Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
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