Table 4 Candidate CNVs with clinical relevance to SGA identified in study placentas
From: Genomic imbalances in the placenta are associated with poor fetal growth
Case ID | Sex | Study group | Genomic coordinates (hg19) | Size (kb) | CNV type | Genes | Category | CPM |
|---|---|---|---|---|---|---|---|---|
7665 | Female | SGA | 2:121,092,278–121,914,455 | 822 | Gain | INHBB, GLI2 | VUS-likely pathogenic | No |
6234 | Female | SGA | 16:67,150,183–67,615,830 | 466 | Loss | HSD11B2, CTCF, 21 others | VUS-likely pathogenic | No |
10506 | Female | SGA | 8:112,947,262–116,124,691 | 3177 | Loss | CSMD3 | VUS-likely pathogenic | No |