Variant DetailsVariant: esv3595770![](http://dgv.tcag.ca/gb2/gbrowse_img/dgv2_hg38/?name=chr3:32297309..32298230;width=800;overview=1) Internal ID | 6636044 | Landmark | | Location Information | | Cytoband | 3p22.3 | Allele length | Assembly | Allele length | hg38 | 922 | hg19 | 922 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv10975031, essv10975016, essv10975014, essv10975027, essv10975038, essv10975025, essv10975026, essv10975019, essv10975012, essv10975017, essv10975041, essv10975023, essv10975036, essv10975010, essv10975033, essv10975045, essv10975022, essv10975035, essv10975039, essv10975030, essv10975011, essv10975046, essv10975034, essv10975020, essv10975018, essv10975048, essv10975029, essv10975042, essv10975047, essv10975015, essv10975024, essv10975040, essv10975044, essv10975043, essv10975032, essv10975013, essv10975037, essv10975021, essv10975028 | Samples | NA12814, HG04158, NA12045, HG00181, HG01704, HG01522, HG00337, HG02407, NA20795, HG00736, NA07347, NA20759, NA12156, HG00309, NA20811, NA12748, HG01524, HG00282, HG01515, NA20536, HG02108, NA20767, HG01092, HG01504, HG01383, HG00117, NA20799, NA19440, HG01357, HG01174, NA20792, HG00256, HG02238, HG01631, NA20758, HG04171, NA20502, HG01756, HG01516 | Known Genes | CMTM8 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3595770
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 39 | Observed Complex | 0 | Frequency | n/a |
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