Variant DetailsVariant: esv3614091 | Internal ID | 7000986 | | Landmark | | | Location Information | | | Cytoband | 7q21.13 | | Allele length | | Assembly | Allele length | | hg38 | 10661 | | hg19 | 10661 |
| | Variant Type | CNV loss | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv12882342, essv12882236, essv12882218, essv12882324, essv12882310, essv12882346, essv12882243, essv12882227, essv12882267, essv12882341, essv12882316, essv12882326, essv12882291, essv12882214, essv12882313, essv12882289, essv12882265, essv12882319, essv12882263, essv12882229, essv12882290, essv12882235, essv12882306, essv12882331, essv12882293, essv12882261, essv12882308, essv12882287, essv12882256, essv12882219, essv12882336, essv12882284, essv12882335, essv12882295, essv12882264, essv12882269, essv12882238, essv12882288, essv12882322, essv12882225, essv12882270, essv12882228, essv12882302, essv12882221, essv12882217, essv12882241, essv12882294, essv12882273, essv12882307, essv12882329, essv12882215, essv12882328, essv12882314, essv12882344, essv12882333, essv12882296, essv12882260, essv12882285, essv12882300, essv12882268, essv12882315, essv12882274, essv12882250, essv12882332, essv12882320, essv12882286, essv12882216, essv12882231, essv12882345, essv12882257, essv12882338, essv12882334, essv12882280, essv12882224, essv12882275, essv12882347, essv12882247, essv12882292, essv12882271, essv12882279, essv12882232, essv12882220, essv12882321, essv12882305, essv12882255, essv12882248, essv12882327, essv12882337, essv12882301, essv12882252, essv12882246, essv12882258, essv12882222, essv12882330, essv12882297, essv12882233, essv12882340, essv12882325, essv12882317, essv12882234, essv12882254, essv12882278, essv12882239, essv12882318, essv12882304, essv12882213, essv12882237, essv12882283, essv12882282, essv12882272, essv12882343, essv12882276, essv12882251, essv12882249, essv12882309, essv12882311, essv12882230, essv12882298, essv12882299, essv12882262, essv12882259, essv12882242, essv12882244, essv12882339, essv12882277, essv12882266, essv12882281, essv12882323, essv12882245, essv12882240, essv12882223, essv12882303, essv12882226, essv12882253, essv12882312 | | Samples | NA18745, HG00235, HG00121, HG03652, HG01965, HG01303, HG00102, NA18947, HG00351, NA20899, HG02433, NA12843, NA11933, HG00233, HG00452, NA19777, NA19684, HG01971, HG03895, HG01518, HG00261, HG00097, HG03950, NA12341, HG01341, HG01506, HG01325, HG01070, NA20798, NA19764, HG03808, NA19771, HG01528, HG00355, HG01510, HG03762, HG00139, HG02493, HG01069, HG03910, HG01398, HG01067, NA20518, HG01519, HG01072, HG01767, HG01673, NA12815, HG01440, HG01048, NA12828, HG00178, HG00253, NA19789, NA20755, NA20753, NA10847, HG00137, NA20904, HG00268, NA19707, HG02233, HG03787, HG03644, NA21119, HG00190, HG02397, HG01095, HG00701, HG04195, HG01515, HG00101, NA20536, HG02253, HG02322, HG03771, HG00275, NA20767, NA18534, HG00551, HG00619, HG01092, HG01447, HG03742, HG01615, HG04054, HG02604, HG01130, HG00321, HG03854, HG03745, HG00704, HG00141, HG04159, NA12778, NA12546, HG01589, HG03743, HG00407, NA20872, NA12716, HG04216, HG01678, NA19072, HG04186, HG00375, HG01362, NA20804, HG01623, NA20792, HG01205, NA20902, NA19439, HG01620, NA12763, HG04003, HG01395, HG00111, NA20582, NA21102, HG01783, HG00112, NA19080, HG01468, HG03611, HG01125, HG01566, HG00759, NA12154, HG04061, HG01786, NA20754, HG01437, HG00978, NA11832 | | Known Genes | | | Method | Sequencing | | Analysis | | | Platform | Multiple platforms | | Comments | | | Reference | 1000_Genomes_Consortium_Phase_3 | | Pubmed ID | 21293372 | | Accession Number(s) | esv3614091
| | Frequency | | Sample Size | 2504 | | Observed Gain | 0 | | Observed Loss | 135 | | Observed Complex | 0 | | Frequency | n/a |
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