Fig. 3
From: Characteristics and clinical evaluation of X chromosome translocations
A The karyotype was 46,X,der(X)t(X;Y)(p22.3;q11.2) for case 6. B Heterochromatin visualized and ligated to Xp22.3 in the C-band for case 6. C The karyotype was 46,X,der(X)t(X;Y)(p22.3;q11.2) for case 7. D CNV-seq revealed seq[GRCh37]Xp22.33p22.31(990,745–6426956) × 1 chrX:g.990745-6426956del chrY: 16,207,792–28819361 for case 6. E CNV-seq revealed seq[GRCh37]del(X)(p22.33p22.33) chrX:g.287328-2757513del seq[GRCh37]dup(Y)(q11.21q12) chrY:g.14567885-28819361dup for the foetus of case 7