High-resolution mapping and analysis of copy number variations in the human genome: A data resource for clinical and research applications

Click on image to view larger version.

Table 3.

Assessment of CNVs detected in a patient with multiple congenital anomalies

Click on table to view larger version.

Table 3.

  • (OR gene) Olfactory receptor gene; (SD region) region of known segmental duplication (RefSeq gene transcript overlap was used for gene assessment); (P.T.) parental transmission. Boldface indicates the putative pathogenic CNV.

This Article

  1. Published in Advance July 10, 2009, doi: 10.1101/gr.083501.108 Genome Res. 19: 1682-1690

Preprint Server



Current Issue

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