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Fig. 1 | Molecular Cytogenetics

Fig. 1

From: Analysis of chromosome 22q11 copy number variations by multiplex ligation-dependent probe amplification for prenatal diagnosis of congenital heart defect

Fig. 1

MLPA analysis of chromosome 22q11 in fetuses 1–11. Probe names are shown on the x-axis. Their chromosomal location is displayed in the upper panel. Columns corresponding to normalized electropherogram peak areas were calculated using Coffalyser software. a. Typical 22q11.2 deletions located from LCR-A to LCR-D regions in fetus 1–6. b. 22q11.2 deletions located from LCR-A to LCR-B regions in fetus 7. c. The deletion located in the 22q11 cat-eye-syndrome region in fetus 8. d. 22q11.2 duplication in fetus 9. e. 22q13.3 deletion in fetus 10. f. 17p13.3 deletion in fetus 11

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Molecular Cytogenetics

ISSN: 1755-8166