Variant DetailsVariant: esv2758526![](http://dgv.tcag.ca/gb2/gbrowse_img/dgv2_hg18/?name=chr20:61572793..61846811;width=800;overview=1) Internal ID | 9633985 | Landmark | | Location Information | | Cytoband | 20q13.33 | Allele length | Assembly | Allele length | hg38 | 274019 | hg19 | 274019 | hg18 | 274019 | hg17 | 274019 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | esv2758806 | Supporting Variants | essv22079, essv17822, essv14315, essv24431, essv15209, essv2238, essv10908, essv9633, essv4364, essv9804, essv17592, essv8913, essv20286, essv10775, essv14607, essv12228, essv7825, essv1888, essv5792, essv23419, essv19190, essv11676, essv16692, essv17260, essv13068, essv22214, essv16107, essv10362, essv14764, essv24679, essv13781, essv22392, essv18399, essv14460, essv19684, essv21405, essv23969, essv11763, essv12967, essv10658, essv21246, essv1105, essv12534, essv13624, essv4017, essv13162, essv15695, essv20613, essv24290, essv15486, essv13884, essv12688, essv24841, essv16905, essv21222, essv22944, essv9876, essv22629, essv10080, essv3029, essv9709, essv17631, essv11212, essv23673, essv14561, essv20179, essv17336, essv13483, essv16983, essv14069, essv24156, essv22768, essv24966, essv12739, essv24572, essv17880, essv4768, essv21681, essv7076, essv18612, essv18082, essv22111, essv23348, essv20339, essv1438, essv21146, essv21511, essv23583, essv20389, essv1533, essv23215, essv9325, essv18252, essv17113, essv15109, essv19793, essv4300, essv19624, essv6356, essv14854, essv21837, essv18227, essv8321, essv5536, essv9194, essv6042, essv22923, essv16267, essv16003, essv19401, essv17710, essv3394, essv23941, essv22569, essv20121, essv1794 | Samples | NA19141, NA19222, NA11830, NA11829, NA19204, NA18861, NA12814, NA18980, NA18855, NA12236, NA19145, NA18603, NA18504, NA12248, NA12865, NA10857, NA19098, NA12750, NA12155, NA07357, NA19127, NA19192, NA19171, NA18944, NA19201, NA10835, NA10846, NA10854, NA18558, NA11992, NA18571, NA12762, NA18964, NA18970, NA07019, NA12156, NA12044, NA19128, NA18966, NA12815, NA19159, NA10855, NA19209, NA10839, NA19200, NA10847, NA12760, NA12752, NA19194, NA12753, NA12003, NA10863, NA10831, NA12872, NA19161, NA18859, NA19205, NA18529, NA19103, NA18976, NA18503, NA11839, NA18981, NA12234, NA19202, NA18537, NA18566, NA18573, NA19142, NA11840, NA10830, NA18856, NA12249, NA18912, NA19154, NA18853, NA12264, NA12145, NA19099, NA12707, NA19101, NA07345, NA12144, NA18523, NA10856, NA18945, NA19094, NA18914, NA12716, NA18863, NA12057, NA18913, NA19100, NA12873, NA19144, NA07348, NA18501, NA12740, NA19093, NA18500, NA18609, NA19102, NA12875, NA18854, NA18852, NA07056, NA18505, NA19129, NA12006, NA07000, NA18522, NA12154, NA19153, NA11832, NA18620, NA18997 | Known Genes | ARFRP1, C20orf195, EEF1A2, GMEB2, HELZ2, KCNQ2, LIME1, PPDPF, PTK6, RTEL1, RTEL1-TNFRSF6B, SLC2A4RG, SRMS, STMN3, TNFRSF6B, ZBTB46, ZGPAT | Method | BAC aCGH | Analysis | Array images were acquired using an Agilent laser scanner (Agilent Technologies, UK). Fluorescence intensities and log2 ratio values were extracted using Bluefuse software (Bluegnome Ltd). | Platform | Agilent | Comments | | Reference | Redon_et_al_2006 | Pubmed ID | 17122850 | Accession Number(s) | esv2758526
| Frequency | Sample Size | 270 | Observed Gain | 3 | Observed Loss | 113 | Observed Complex | 0 | Frequency | n/a |
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