Spectrum of large copy number variations in 26 diverse Indian populations: potential involvement in phenotypic diversity
Copy number variations (CNVs) have provided a dynamic aspect to the apparently static human genome. We have analyzed CNVs larger than 100 kb in 477 healthy individuals from 26 diverse Indian populations of different linguistic, ethnic and geographic backgrounds. These CNVRs were identified using the...
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Veröffentlicht in: | Human genetics 2012, Vol.131 (1), p.131-143 |
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