Variant DetailsVariant: dgv633e199 Internal ID | 20123935 | Landmark | | Location Information | | Cytoband | 19p12 | Allele length | Assembly | Allele length | hg38 | 1073157 | hg19 | 1073157 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | esv2664371, esv2669125, esv2671513, esv2660015 | Samples | NA19909, HG00384, NA18565, HG00306, NA19057, NA18616, NA18870, NA18567, NA18619, HG01492, NA18618, NA12283, NA18498, NA18964, NA19130, NA18949, NA18611, NA18874, NA19372, HG01440, NA19901, NA20755, HG00464, NA19007, NA20800, HG00266, NA19236, HG00740, HG01047, HG01383, NA12827, NA18945, HG00155, NA19434, NA20504, NA20803, HG01342, NA06986, NA20807, NA20758, NA19463, NA18511, NA18622, NA18965, NA18577 | Known Genes | LOC100996349, LOC440518, ZNF208, ZNF257, ZNF492, ZNF676, ZNF728, ZNF729, ZNF98, ZNF99 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | dgv633e199
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 45 | Observed Complex | 0 | Frequency | n/a |
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