Variant DetailsVariant: esv2665441Internal ID | 9584860 | Landmark | | Location Information | | Cytoband | 5q15 | Allele length | Assembly | Allele length | hg38 | 555 | hg19 | 555 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5415290, essv6083064, essv5700892, essv6417263, essv6350614, essv6002564, essv5821823, essv5713129, essv6199039, essv5779927, essv6044300, essv6169455, essv6473316, essv5650023, essv6214282, essv5851558, essv5468358, essv5822133, essv6193113 | Samples | NA18508, NA18980, NA19190, NA18519, NA18942, NA18916, NA19138, NA18498, NA19239, NA19210, NA19455, NA18523, NA19834, NA18952, NA18517, NA19240, NA19129, NA19463, NA18965 | Known Genes | TTC37 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2665441
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 19 | Observed Complex | 0 | Frequency | n/a |
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