Variant DetailsVariant: esv2665113 Internal ID | 9584532 | Landmark | | Location Information | | Cytoband | 6q26 | Allele length | Assembly | Allele length | hg38 | 3040 | hg19 | 3040 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv1167e199 | Supporting Variants | essv6069823, essv6001899, essv5693831, essv5606231, essv6253391, essv5755517, essv5899801, essv6044867, essv5499795, essv6567183, essv6392100, essv5691770, essv5840938, essv5674833, essv5670771, essv6345024, essv5498917, essv5964056, essv6325765, essv5497764, essv6553270, essv5768967, essv5435122, essv5791989, essv6022269, essv6399705, essv5861299, essv5942835, essv5645564, essv5494091, essv5965474, essv6217532, essv5623533, essv5795377, essv6544879, essv6275319, essv5805302, essv5737042, essv5925390, essv5694236, essv6562158, essv6146168, essv6577791, essv6453525, essv5836089, essv5766593, essv6106618, essv6475979, essv6024902, essv5588422, essv5484806, essv6211691, essv5402105, essv5575229, essv5879100, essv5840535, essv6274319, essv5900913, essv6003442, essv6533343, essv6012733, essv5469185, essv5693059, essv6536824, essv6435340, essv6177802, essv5886127, essv5601680, essv5399537, essv6394178, essv5716740, essv5572423, essv6352488, essv5741073, essv6485548, essv5444828, essv5688424, essv6156434, essv6147355, essv6412487, essv5477607, essv6513938, essv5796665, essv5529038, essv6018869, essv6305135, essv6571683, essv5980761, essv5774116, essv5545765, essv6221659, essv5410079, essv6400308, essv5494912, essv5511337, essv6369024, essv5745341, essv6365778, essv5565499, essv5758196, essv6349074, essv6229967, essv5551115, essv5561543, essv6412141 | Samples | HG00096, HG00189, NA19648, HG00143, NA19397, NA19466, NA11829, NA19399, NA19332, HG01079, NA11920, NA20294, NA19355, NA19393, HG00566, NA19377, HG00737, HG01461, NA19443, HG01051, NA18633, NA12155, NA12341, HG01250, NA19396, NA19381, NA19373, NA19379, HG01366, NA19448, NA19678, NA20774, NA20317, NA19916, HG00330, HG01365, HG00334, NA19782, NA19384, NA19079, NA19720, NA19383, NA20819, HG00232, NA19372, NA19371, NA19471, HG01440, NA19189, HG01048, HG01133, HG00253, NA19921, HG01124, HG00133, HG01136, HG00188, NA19908, NA19247, HG00268, HG01384, NA19403, NA20809, NA19455, NA19236, NA19982, NA12718, NA18910, HG00690, HG00404, HG01197, NA19453, NA19338, NA19395, NA20534, NA19440, NA19390, NA18909, NA19434, HG00366, NA19473, HG00136, NA19435, NA19444, HG00278, NA20792, NA19428, NA20544, HG00319, HG01108, NA12347, NA19398, NA18631, NA19438, NA19468, HG00280, NA19213, NA19661, NA19430, NA19755, NA18511, NA18612, NA19429, HG01437, NA19431 | Known Genes | PARK2 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2665113
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 105 | Observed Complex | 0 | Frequency | n/a |
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