Variant DetailsVariant: esv2678342 Internal ID | 9597761 | Landmark | | Location Information | | Cytoband | 10q23.31 | Allele length | Assembly | Allele length | hg38 | 900 | hg19 | 900 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5683514, essv5644029, essv6232032, essv6292997, essv5699070, essv5711949, essv6354563, essv6146367, essv6111282, essv6537371, essv6517659, essv5789183, essv5632254, essv5498114, essv5734052, essv5685819, essv6163459, essv5775886, essv5564303, essv6036018, essv5533971, essv6299006, essv6259036, essv5471642, essv5669711, essv6037572, essv5674857 | Samples | HG01441, NA10851, NA12414, NA20532, HG00150, HG00271, NA07346, NA12287, HG00247, NA19384, NA19404, NA20539, HG00277, NA20538, HG00141, NA12043, HG00375, NA07051, HG00237, NA19470, NA06986, HG00339, NA19716, HG00267, NA07000, HG01191, HG01437 | Known Genes | PTEN | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | High quality site | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2678342
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 27 | Observed Complex | 0 | Frequency | n/a |
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