Variant DetailsVariant: esv3608563 Internal ID | 6648796 | Landmark | | Location Information | | Cytoband | 6p21.33 | Allele length | Assembly | Allele length | hg38 | 46767 | hg19 | 46767 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv12262570, essv12262621, essv12262583, essv12262601, essv12262581, essv12262591, essv12262559, essv12262599, essv12262602, essv12262552, essv12262580, essv12262586, essv12262605, essv12262575, essv12262558, essv12262616, essv12262553, essv12262562, essv12262573, essv12262597, essv12262566, essv12262611, essv12262579, essv12262578, essv12262613, essv12262574, essv12262598, essv12262577, essv12262567, essv12262564, essv12262557, essv12262568, essv12262620, essv12262572, essv12262610, essv12262588, essv12262576, essv12262561, essv12262619, essv12262549, essv12262563, essv12262550, essv12262556, essv12262623, essv12262569, essv12262614, essv12262606, essv12262600, essv12262571, essv12262612, essv12262594, essv12262555, essv12262582, essv12262589, essv12262565, essv12262622, essv12262585, essv12262554, essv12262551, essv12262603, essv12262617, essv12262560, essv12262596, essv12262615, essv12262595, essv12262618, essv12262607, essv12262593, essv12262587, essv12262584, essv12262604, essv12262609, essv12262590, essv12262608, essv12262592 | Samples | NA18745, HG02628, HG03378, HG01303, NA19664, HG00671, HG02298, HG02433, HG02150, NA19795, HG03193, HG01051, HG03572, NA18563, NA19201, NA19764, HG01167, HG00689, HG02146, NA19723, NA18982, NA19198, NA18558, NA19649, HG02299, NA19771, NA19681, NA19079, NA19720, NA20340, HG01849, HG01369, NA19921, HG03861, HG01871, HG00557, HG02057, HG02253, HG00436, HG00533, HG02508, HG01102, NA20867, HG04054, HG01921, HG04017, NA19740, HG04063, NA19761, HG02286, NA18536, HG01572, NA19401, NA19729, HG04188, NA19149, HG02546, HG02308, NA19732, HG01939, HG01375, HG03108, NA19759, HG03025, HG02291, NA19080, NA19780, HG01794, NA19146, NA19758, HG04056, HG02425, HG02006, HG01578, NA18620 | Known Genes | HCG26, HCP5 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3608563
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 75 | Observed Complex | 0 | Frequency | n/a |
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