Variant DetailsVariant: esv3636025 Internal ID | 6676134 | Landmark | | Location Information | | Cytoband | 15q13.2 | Allele length | Assembly | Allele length | hg38 | 71453 | hg19 | 71453 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv15203627, essv15203641, essv15203643, essv15203640, essv15203639, essv15203626, essv15203644, essv15203623, essv15203624, essv15203642, essv15203628, essv15203637, essv15203636, essv15203631, essv15203630, essv15203638, essv15203634, essv15203635, essv15203646, essv15203632, essv15203647, essv15203629, essv15203633, essv15203645, essv15203625 | Samples | HG04210, NA11830, NA18999, NA18528, HG00244, HG01802, NA19057, NA12813, NA18960, NA19054, NA18964, HG03595, HG02260, NA18985, HG01709, NA18973, NA18747, NA19077, NA18981, HG01512, HG03790, HG01894, NA18972, HG01377, HG00759 | Known Genes | ARHGAP11B, LOC100288637 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3636025
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 25 | Observed Complex | 0 | Frequency | n/a |
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