Variant DetailsVariant: esv3627311 Internal ID | 6667459 | Landmark | | Location Information | | Cytoband | 11q21 | Allele length | Assembly | Allele length | hg38 | 9446 | hg19 | 9446 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv14241747, essv14241744, essv14241776, essv14241741, essv14241762, essv14241736, essv14241765, essv14241727, essv14241732, essv14241780, essv14241782, essv14241778, essv14241788, essv14241755, essv14241750, essv14241769, essv14241735, essv14241722, essv14241772, essv14241781, essv14241749, essv14241760, essv14241770, essv14241779, essv14241757, essv14241721, essv14241766, essv14241763, essv14241751, essv14241739, essv14241759, essv14241764, essv14241734, essv14241731, essv14241745, essv14241730, essv14241777, essv14241738, essv14241775, essv14241773, essv14241733, essv14241742, essv14241783, essv14241787, essv14241771, essv14241785, essv14241754, essv14241761, essv14241740, essv14241729, essv14241786, essv14241743, essv14241737, essv14241728, essv14241753, essv14241767, essv14241726, essv14241774, essv14241748, essv14241724, essv14241723, essv14241752, essv14241758, essv14241756, essv14241725, essv14241768, essv14241746, essv14241784 | Samples | HG01985, NA20339, HG02890, HG02496, NA19703, HG02481, NA18881, HG03455, NA18878, HG03100, HG03126, NA20346, HG03172, HG03074, HG03874, HG02054, NA19904, HG02816, HG02143, HG03520, HG02703, HG02561, HG01369, HG03195, NA19317, NA19901, HG02427, NA19209, NA20127, HG03369, HG02479, NA19184, HG02511, NA19913, NA19236, HG03575, HG03294, HG03563, HG02429, NA18879, HG03397, HG02283, HG03024, HG03451, NA18858, HG01896, NA19436, HG02455, NA19434, HG02308, HG02923, NA19439, HG03084, NA20357, NA20348, HG02095, HG02107, HG03063, HG01883, HG03445, NA19430, HG02861, HG03856, HG01886, HG03118, HG02006, NA19214, NA19153 | Known Genes | PANX1 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3627311
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 68 | Observed Complex | 0 | Frequency | n/a |
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