Copy number variation: New insights in genome diversity

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Figure 6.
Figure 6.

Cross-platform identification and validation of CNVs. (A) Array CGH, (B) Nimblegen array, (C) Agilent array, and (D) Affymetrix 500k SNP array platforms all identifying copy number variants in the GM 15510 individual from whom the G248 fosmid DNA library, used in the Tuzun et al. (2005) study, was created.

This Article

  1. Published in Advance June 29, 2006, doi: 10.1101/gr.3677206 Genome Res. 16: 949-961

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