Variant DetailsVariant: esv3603109Internal ID | 6643365 | Landmark | | Location Information | | Cytoband | 4q32.3 | Allele length | Assembly | Allele length | hg38 | 813 | hg19 | 813 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv11687760, essv11687755, essv11687761, essv11687763, essv11687754, essv11687758, essv11687757, essv11687764, essv11687759, essv11687762, essv11687753, essv11687756 | Samples | HG02583, NA19704, HG02624, HG02589, HG03460, HG02703, NA19209, HG03391, HG02484, HG01915, NA19474, HG02855 | Known Genes | PALLD | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3603109
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 12 | Observed Complex | 0 | Frequency | n/a |
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