Fig. 1
From: Molecular and cytogenetic analysis of small supernumerary marker chromosomes in prenatal diagnosis
The morphology and idiograms of sSMCs with abnormal CMA results. Case 3: arr[hg19] 13q11q12.12(19,436,286–25,319,733) × 3; Case 5: arr[hg19] 12p13.33p11.1(173,786–34,835,641) × 4; Case 6: arr[hg19] 15q11.2q13.3(22,770,421-32,915,723) × 4; Case 7: arr[hg19] Xp22.33p11.22(168,551-52,877,319) × 1,Xp11.22q21.1(52,877,320–77,345,323) × 1–2,Xq21.1q28(77,345,324-155,233,098) × 1; Case 9: arr[hg19] 6p25.3(156,974–889,487) × 3,15q11.2q13.2(22,770,421–30,913,574) × 3; Case 11: arr[hg19] Xp22.33q11.1(168,551–62,051,248) × 1,Xq11.2q12(63,002,581–65,354,853) × 1,Xq21.1q28(80,602,173-155,233,098) × 1; Case 12: arr[hg19] Xp22.33p11.21(168,551-57,677,734) × 1–2,Xp11.21q11.2(57,677,735–63,489,866) × 2–3,Xq12q13.1(67,062,445-68,992,710) × 2-3,Xq13.1q28(68,992,711-155,233,098) × 1–2; Case 13: arr[hg19] 15q11.2q13.3(22,770,421-32,915,723) × 4; Case 15: arr[hg19] 12p13.33q11(173,786–37,858,351) × 4; Case 17: arr[hg19] Xp22.33p11.21(168,551_58,527,154) × 1,Xp11.21q21.1(58,527,155_80,103,965) × 1–2, Xq21.1q28(80,103,966_155,233,098) × 1; Case 20: arr[hg19] 15q11.2q13.3(22,770,422_32,444,261) × 4; Case 21: arr[hg19] Xp22.33p11.1(168,551–58,112,823) × 1,Xq13.3q28(75,024,481–155,233,098) × 1; Case 22: arr[hg19] Xp22.33p11.3(168,551–45,446,616) × 1,Xp11.3q13.3(45,518,515–75,045,175) × 1–2,Xq13.3q28(75,404,909–155,233,098) × 1; Case 23: arr[hg19] 9p24.3p13.1(208,454–38,787,480) × 3; Case 24: arr[hg19] 18p11.32p11.21(136,227–15,181,208) × 2–3; Case 25: arr[hg19] Yp11.31q11.21(2,650,424–14,736,209) × 0–1,Yq11.21q11.23(14,736,210–28,799,654) × 0