Variant DetailsVariant: essv3574981Internal ID | 6699677 | Landmark | | Location Information | | Cytoband | 18p11.32 | Allele length | Assembly | Allele length | hg38 | 147 | hg19 | 147 | hg18 | 147 |
| Variant Type | CNV deletion | Copy Number | | Allele State | Homozygous | Allele Origin | Not tested | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv1007840 | Supporting Variants | | Samples | HuRef | Known Genes | EMILIN2 | Method | Sequencing | Analysis | | Platform | Sanger Sequencing | Comments | | Reference | Pang_et_al_2010 | Pubmed ID | 20482838 | Accession Number(s) | essv3574981
| Frequency | Sample Size | 3 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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