Prediction of a deletion copy number variant by a dense SNP panel
<p>Abstract</p> <p>Background</p> <p>A newly recognized type of genetic variation, Copy Number Variation (CNV), is detected in mammalian genomes, e.g. the cattle genome. This form of variation can potentially cause phenotypic variation. Our objective was to determine wh...
| Main Authors: | , , |
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| Format: | Article |
| Language: | deu |
| Published: |
BMC
2012-03-01
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| Series: | Genetics Selection Evolution |
| Online Access: | http://www.gsejournal.org/content/44/1/7 |