Variant DetailsVariant: esv3613765 Internal ID | 6653973 | Landmark | | Location Information | | Cytoband | 7q11.23 | Allele length | Assembly | Allele length | hg38 | 15245 | hg19 | 15245 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv12848894, essv12848910, essv12848921, essv12848908, essv12848895, essv12848893, essv12848909, essv12848899, essv12848916, essv12848901, essv12848915, essv12848912, essv12848898, essv12848913, essv12848900, essv12848919, essv12848897, essv12848903, essv12848917, essv12848902, essv12848920, essv12848904, essv12848907, essv12848918, essv12848911, essv12848905, essv12848892, essv12848914, essv12848922, essv12848906, essv12848896 | Samples | HG03057, HG03963, NA19198, HG03736, NA19138, NA18498, HG02816, NA12005, HG02642, HG01198, HG02477, NA19175, HG01882, HG03428, HG03446, HG02283, HG02594, NA19834, HG02314, NA19328, NA19117, HG03157, HG01917, HG02367, NA19351, HG03313, HG02938, HG02676, HG02947, NA19146, HG02343 | Known Genes | DTX2, UPK3B | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3613765
| Frequency | Sample Size | 2504 | Observed Gain | 31 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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