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Fig. 2 | Molecular Cytogenetics

Fig. 2

From: Non-invasive prenatal screening for Emanuel syndrome

Fig. 2

CMA confirmed the duplication. (a) CMA for fetus of case 1 reveals approximately 18.2 Mb duplication in chromosome 11q23.3q25 (chr11:116,696,886-134,938,470).(b) CMA for fetus of case 1 reveals 3.2 Mb duplication in chromosome 22q11.1q11.21 chr 22:17,055,733-20,311,858).(c) In case 2, an approximately 18.2 Mb duplication in chromosome11q23.3q25(chr11:116,681,007-134,938,470) .(d) In case 2, 3.4 Mb duplication in chromosome 22q11.1q11.21. The horizontal axis represents genomic location (Mb). The blue rectangle represents the duplication

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Molecular Cytogenetics

ISSN: 1755-8166