Abstract
Approximately 12% of the human genome consists of relatively common copy number variations (CNVs) — i.e., insertions or duplications of DNA sequences
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Published version (
Free)
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
