Variant DetailsVariant: esv3094901| Internal ID | 10767881 | | Landmark | | | Location Information | | | Cytoband | 19p13.12 | | Allele length | | Assembly | Allele length | | hg38 | 1798 | | hg19 | 1798 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv7364468 | | Samples | HuRef | | Known Genes | EMR3 | | Method | Sequencing | | Analysis | | | Platform | Complete Genomics | | Comments | | | Reference | Pang_et_al_2013b | | Pubmed ID | 24192839 | | Accession Number(s) | esv3094901
| | Frequency | | Sample Size | 1 | | Observed Gain | 0 | | Observed Loss | 1 | | Observed Complex | 0 | | Frequency | n/a |
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