Fig. 3 | Scientific Reports

Fig. 3

From: Prenatal diagnosis of imprinted associated chromosome abnormalities identified by noninvasive prenatal testing (NIPT)

Fig. 3

Results of genetic tests in P8 and P9. A. The G-band karyotype of the P8 fetus was normal. B and C CMA of the amniotic fluid indicated maternal loss of heterozygosity at 6q25.2q27: arr[GRCh37] 6q25.2q27(152902809_170896644)x2 hmz. The CAM result of P8 was normal. D and E The CMA results of the P9 fetus indicated loss of heterozygosity at 15q23q25.3: arr[GRCh37]15q23q25.3(70673857_86592054)×2 hmz. MLPA (ME028) revealed that the 15q11 chromosomal region in P9:F copy number ratio was approximately 1, and the G methylation ratio was normal.

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