Variant DetailsVariant: esv1010432| Internal ID | 6722521 | | Landmark | | | Location Information | | | Cytoband | 11q24.1 | | Allele length | | Assembly | Allele length | | hg38 | 14525 | | hg19 | 14525 | | hg18 | 14525 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv3563560 | | Samples | HuRef | | Known Genes | GRAMD1B | | Method | Sequencing | | Analysis | | | Platform | Sanger Sequencing | | Comments | | | Reference | Pang_et_al_2010 | | Pubmed ID | 20482838 | | Accession Number(s) | esv1010432
| | Frequency | | Sample Size | 3 | | Observed Gain | 0 | | Observed Loss | 1 | | Observed Complex | 0 | | Frequency | n/a |
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