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
- 30 Jun 2011
Genome-wide Studies of Copy Number Variation and Exome Sequencing Identify Rare Variants in BAG3 as a Cause of Dilated Cardiomyopathy
Learn | Publications
- Sep 2011 | Cell
Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangements. - Jun 2011 | Neuron
Rare de novo and transmitted copy-number variation in autistic spectrum disorders. - May 2011 | Appl Environ Microbiol
Comparative genomics of Escherichia coli strains causing urinary tract infections. - April 2011 | Fertil Steril
Complex X chromosome rearrangement delineated by array comparative genome hybridization in a woman with premature ovarian insufficiency.
