Incidental detection of cancer predisposition gene copy number variations by array comparative genomic hybridization

Academic Article

Abstract

  • © 2014 Elsevier Inc. All rights reserved. We describe 2 pediatric patients who presented to medical genetics clinic for evaluation and were incidentally found via array comparative genomic hybridization to have pathogenic copy number variations of cancer predisposition genes. We subsequently reviewed 3554 previous array comparative genomic hybridization results to estimate the frequency of similar incidental findings.
  • Published In

    Digital Object Identifier (doi)

    Author List

  • Hamm JA; Mikhail FM; Hollenbeck D; Farmer M; Robin NH
  • Start Page

  • 1057
  • End Page

  • 1059.e4
  • Volume

  • 165
  • Issue

  • 5