Copy Number Variation (CNV) Arrays
With the emergence of high-resolution maps of CNVs, their impact on disease phenotypes has become a key research focus. Life science researchers are rapidly adopting the use of CNV arrays for large-scale genome-wide association studies. To facilitate this effort, Roche NimbleGen has developed Human CNV arrays in 2.1M and 3x720K array formats for comprehensive and high-resolution analysis of genome-wide CNVs.
Learn | Literature
- NimbleGen Copy Number Variation (CNV) Arrays
Datasheet (PDF Format 1.4MB) - Descriptions of HG18 and HG19 Annotation Files (Version 3.0)
Datasheet (PDF Format 409KB) - Human Genome HG19 Annotation Files
Annotation Files (ZIP Format 12.8MB)
What files are included in this download? - Human Genome HG18 Annotation Files
Annotation Files (ZIP Format 11.2MB)
What files are included in this download? - Detecting Copy Number Variants Associated with Basal Cell Carcinoma in an Arsenic-Exposed Population
Application Note (PDF Format 1.2MB) - High Resolution Copy Number Analysis of Parkinson’s Samples Using Nexus Copy Number and Roche NimbleGen Microarrays
Whitepaper (PDF Format 964KB)
Learn | Webinars
- ASHG 2010
Identification of a Novel Locus Associated with the Common Birth Defect Spina Bifida
- ASHG 2010
Exonic aCGH for Copy Number Detection in Mitochondrial Diseases
Learn | Publications
- Jun 2010 | Blood
Telomere dysfunction and fusion during the progression of chronic lymphocytic leukaemia: evidence for a telomere crisis. - May 2010 | BMC Genomics
Copy number variation in the bovine genome. - Nov 2009 | Clin Cancer Res
Homozygous deletion of MTAP gene as a poor prognosticator in gastrointestinal stromal tumors. - Nov 2009 | Nat Genet
T (brachyury) gene duplication confers major susceptibility to familial chordoma.
