Table 3 Summary of the results of the tiling path microarray comparative genomic hybridisation analysis
GainsLosses
ChrCytobandStart (Mb)End (Mb)CNV*CNV typeChrCytobandStart (Mb)End (Mb)CNV*CNV type
44p6.3–p16.20.663.62YesMainly deletion66q24.1–q27142.51169.41
44p16.16.337.31YesMainly deletion1212p13.2–q1211.9538.70
55p15.330.431.04YesMainly deletion1414q22.3–q23.155.1556.16YesMainly deletion
1010q2143.0145.46No1515q25.3–q26.386.3097.21YesIntermittently
1010q26.3134.41135.25No1919p13.28.638.78YesMainly deletion
1212p13.3–p13.20.0211.86YesYes†
1515q11–q25.318.2786.33
1515q26.2–15q26.395.6096.57YesMainly deletion
1616p13.30.013.51YesMainly deletion
1616p13.3–q24.24.5088.69
1818q2374.3476.10YesMainly deletion
1919p13.31.222.19YesMainly deletion
  • *The presence of copy number variations/polymorphisms was only assessed if the region was ⩽15 Mb, given that the vast majority of these encompass regions <2 Mb.

  • †Multiple copy number variations interspersed with regions without.

  • Chr, chromosome; CNV, copy number variation/polymorphism.