NAHR-mediated copy-number variants in a clinical population: Mechanistic insights into both genomic disorders and Mendelizing traits

(Downloading may take up to 30 seconds. If the slide opens in your browser, select File -> Save As to save it.)

Click on image to view larger version.

Figure 3.
Figure 3.

Known recurrent CNVs found in the MGL BCM CMA database divided into de novo (colored) and inherited (white), excluding ∼75% of events of unknown parental origin (i.e., no parental study was performed). Among de novo events, more deletions were found than reciprocal duplications.

This Article

  1. Published in Advance May 8, 2013, doi: 10.1101/gr.152454.112 Genome Res. 23: 1395-1409

Preprint Server



Current Issue

  1. February 2026, 36 (2)
  1. Current Issue
  1. Alert me to new issues of Genome Research