Variant DetailsVariant: esv3624116 Internal ID | 6664283 | Landmark | | Location Information | | Cytoband | 10q23.31 | Allele length | Assembly | Allele length | hg38 | 901 | hg19 | 901 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13887886, essv13887876, essv13887880, essv13887875, essv13887890, essv13887907, essv13887868, essv13887906, essv13887897, essv13887867, essv13887882, essv13887865, essv13887905, essv13887869, essv13887888, essv13887902, essv13887898, essv13887884, essv13887866, essv13887877, essv13887872, essv13887887, essv13887878, essv13887904, essv13887908, essv13887899, essv13887903, essv13887896, essv13887873, essv13887893, essv13887883, essv13887901, essv13887900, essv13887892, essv13887894, essv13887874, essv13887871, essv13887889, essv13887879, essv13887891, essv13887870, essv13887881, essv13887895, essv13887885 | Samples | HG01441, HG00121, HG00384, NA10851, HG00358, NA12414, HG01537, NA20532, HG00150, HG01632, HG00271, HG00272, NA19319, HG01676, HG00129, HG04131, NA19384, NA19404, NA20539, HG00277, HG04183, HG01455, HG01519, HG01259, HG00743, NA12760, HG01345, HG01504, NA20538, HG00141, NA12043, HG00375, HG01253, NA07051, HG00237, NA06986, HG00339, HG01765, NA19716, HG00267, HG01269, HG01191, HG01437, HG01608 | Known Genes | PTEN | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3624116
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 44 | Observed Complex | 0 | Frequency | n/a |
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