xGen CNV Backbone Panel—Tech Access
Identify copy number variations in your human NGS data
The xGen CNV Backbone Panel—Tech Access spans the entire human genome, allowing you to generate reference coverage data that can be used to detect copy number variations (CNVs). This panel consists of 9115 individually synthesized xGen Lockdown Probes spaced approximately every 0.34 Mb across the genome.
With its convenient modular formulation, the xGen CNV Backbone Panel—Tech Access can be used either as a spike-in addition to other xGen Lockdown Probe panels, such as the xGen Exome Research Panel, or independently for standalone NGS target capture.
- Detect changes in copy number throughout the human genome
- Use as either a spike-in or a standalone panel
- Enjoy fast turnaround via easy online ordering and next day shipping