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Figure 2 | Molecular Cytogenetics

Figure 2

From: Best diagnostic approach for the genetic evaluation of fetuses after intrauterine death in first, second or third trimester: QF-PCR, karyotyping and/or genome wide SNP array analysis

Figure 2

Overview of diagnostic testing in 417 IUFD samples. Aneuploidy testing (by QF-PCR or karyotyping) is categorized as normal, aneuploidy, not performed or failed. Microarray results are indicated as normal (benign CNV), clinically relevant, unknown (CNV of unknown inheritance), inherited (likely/probably benign CNV) or failed. Mono X: monosomy X; *sample tested by QF-PCR and karyotyping; **two samples tested by both QF-PCR and karyotyping.

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