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Fig. 2 | Molecular Cytogenetics

Fig. 2

From: Prenatal diagnosis of complete maternal uniparental isodisomy of chromosome 4 in a fetus without congenital abnormality or inherited disease-associated variations

Fig. 2

Identification of copy number variations. ChAS software indicated a single deletion (red triangle) and a single duplication of CNVs (blue triangle) in the fetal sample (blue arrow). Three duplicated CNVs were observed in the mother (red arrow), whereas only a single duplicated CNV was observed in the father (light blue arrow)

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