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Figure 1 | Molecular Cytogenetics

Figure 1

From: Molecular karyotyping by array CGH in a Russian cohort of children with intellectual disability, autism, epilepsy and congenital anomalies

Figure 1

Examples of array CGH graphical overviews. A. Case #8: a deletion of chromosome X short arm and a duplication of chromosome 3 short arm — arr Xp22.33p22.2(2,333,897-9,726,574)x1,3p26.3p22.3(200,000-36,550,871)x3 — due to an unbalanced maternal translocation t(X;3) (conventional karyotyping was performed after array CGH analysis). B. Case #27: a deletion of chromosome 7 long arm (subtelomeric 7q deletion) — arr 7q36.2q36.3(152,768,630-158,261,821)x1. C. Case #18: a duplication of chromosome 19 short arm — arr 19p13.3(260,000-4,953,188)x3. D. Case #20: a deletion of chromosome 10 long arm (subtelomeric 10q deletion) — arr 10q26.2q26.3(128,192,760-134,070,099)x1. E. Case #40: a duplication of chromosome 5 long arm — arr 5q13.2(68,931,140-72,690,180)x3.

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Molecular Cytogenetics

ISSN: 1755-8166