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Table 1 Summary of array CGH analysis

From: The clinical application of array CGH for the detection of chromosomal defects in 20,126 unselected newborns

 

Cases with abnormal array CGH analysisa

Total (N)

Detection rate (%)

Aneuploidy (N)

Deletion (N)

Duplication (N)

Neonatal casesb

     

(N = 20126)

53

23

11

87

0.43

  1. a array CGH analysis results confirmed by Karyotyping and FISH analyses.
  2. bAll neonatal cases, collected < 0.5 year of age, between 2010–2012.
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Molecular Cytogenetics

ISSN: 1755-8166