Copy Number Variation (CNV) is a deletion/duplication of segments of the genome and varies among individuals. Detection of CNV can be useful for the identification of therapeutic indication in cancer patients and various other genetic disorders. For a detailed explanation of the mathematical calculations for CNV, click here: Copy Number Variation Calculation
This tool automatically estimates the Copy Number Variation (CNV) of targeted genes with respect to reference genes, together with their confidence interval and relative uncertainty for a given confidence level.
Below is an example of common usage. Download it and follow the steps to get the result.
How to use the tool?
- Get the template
- Complete the file with your information
- Post the completed file and click Submit to automatically download results
1 -Download the template
Get an example
2 - Select data