Targeted genomic microarray analysis for identification of chromosome abnormalities in 1500 consecutive clinical cases

J Pediatr. 2006 Jul;149(1):98-102. doi: 10.1016/j.jpeds.2006.02.006.


Objective: To assess the yield of array-based comparative genomic hybridization.

Study design: The results of array comparative genomic hybridization were collected on 1500 consecutive clinical cases sent to our laboratory for a variety of developmental problems. Confirmation fluorescence in situ hybridization of metaphase or interphase cells, depending on the aberration, was performed.

Results: Of the 1500 cases, 134 (8.9%) showed an abnormality: 36 (2.4%) showed polymorphisms or familial variants, 14 (0.9%) showed alterations of unknown clinical significance, and 84 (5.6%) showed clinically relevant genomic alterations. These included subtelomeric deletions and unbalanced rearrangements, microdeletions and reciprocal duplications, rare abnormalities, and low-level trisomy mosaicism.

Conclusions: A targeted array detects a substantial proportion of abnormalities even in those patients who have already had extensive cytogenetic and/or fluorescence in situ hybridization testing. This study, although not a controlled ascertainment of subjects with specific selection criteria, accurately reflects the reality of clinical cytogenetic practice and provides an estimate of the cytogenetic abnormalities that can be identified with a targeted microarray in a diagnostic laboratory. Microarray analysis likely doubles the current yield of abnormal results detected by conventional cytogenetic analysis.

MeSH terms

  • Child
  • Chromosome Aberrations*
  • DNA / analysis
  • Genetic Variation
  • Humans
  • In Situ Hybridization, Fluorescence
  • Nucleic Acid Hybridization
  • Oligonucleotide Array Sequence Analysis / methods*
  • Prospective Studies


  • DNA