Copy number variation (CNV)

A tailored CNV service from the microarray experts

Use our oligonucleotide aCGH service to discover copy number variations in the human genome and their link to disease

Choose from a regular service using standard array designs or let us do the design by harnessing the power of the Oligome™ to give you focussed custom aCGH arrays allowing you to focus on your research project

How does this work?

  • choose your regions of interest
  • we select probes from the Oligome - a database of more than 10 million oligonucleotide probes designed to the latest release of the human genome
  • view the selected probes using the Oligome viewer software, prior to fabrication
  • we print the arrays and either process them in our lab or deliver back to you
  • analyse your data using the Oligome analysis software
    - an easy to use complimentary software tool


CVN service
Custom Contact us

Catalogue
Eukaryote


human
Array formats Click here for illustration of array formats

Learn more zone

Click here to find out more about our CNV application.