Variant DetailsVariant: essv3564524| Internal ID | 6689220 | | Landmark | | | Location Information | | | Cytoband | 20q13.12 | | Allele length | | Assembly | Allele length | | hg38 | 7645 | | hg19 | 7646 | | hg18 | 7646 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | Not tested | | Probe Count | | | Validation Flag | | | Merged Status | S | | Merged Variants | esv990338 | | Supporting Variants | | | Samples | HuRef | | Known Genes | ZMYND8 | | Method | Sequencing | | Analysis | | | Platform | Sanger Sequencing | | Comments | | | Reference | Pang_et_al_2010 | | Pubmed ID | 20482838 | | Accession Number(s) | essv3564524
| | Frequency | | Sample Size | 3 | | Observed Gain | 0 | | Observed Loss | 1 | | Observed Complex | 0 | | Frequency | n/a |
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