All DNA/RNA Services
DNA Whole Genome
CNV
Copy number variants (CNV) make up more than 10% of the human genome. Altered CNV can lead to gene dosage imbalances and change responses to drugs and susceptibility to disease, including Parkinson’s and Alzheimer’s. In addition, researching the mechanisms that lead to CNV formation may provide valuable insight on human genome evolution. EA offers a variety of analysis options for estimating chromosomal copy number changes. These analyses rely on data from the polymorphic and nonpolymorphic markers on the Affymetrix whole-genome microarrays. Results are returned in tabular and/or graphical displays, including an aligned chromosomal view.
Genome-Wide Human SNP Array 6.0
Performance Specs
GeneChip Human Mapping 250k Sty Array
Performance Specs
Mapping 10k 2.0 Array Set
Performance Specs
- RELATED SERVICES
- Whole Genome - CNV
- STEP 2
- BioInformatic Services
- STEP 3
- Applied Biosystems qPCR