Variant DetailsVariant: nsv514897 Internal ID | 15466531 | Landmark | | Location Information | | Cytoband | 19q13.12 | Allele length | Assembly | Allele length | hg38 | 12269 | hg19 | 12269 | hg18 | 12269 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2841701, nssv2841717, nssv2841682, nssv2841679, nssv2841614, nssv2841657, nssv2841595, nssv2841636, nssv2841647, nssv2841660, nssv2841669, nssv2841627, nssv2841707, nssv2841629, nssv2841681, nssv2841663, nssv2841611, nssv2841700, nssv2841648, nssv2841722, nssv2841661, nssv2841658, nssv2841659, nssv2841626, nssv2841645, nssv2841620, nssv2841719, nssv2841641, nssv2841690, nssv2841631, nssv2841723, nssv2841695, nssv2841632, nssv2841688, nssv2841637, nssv2841639, nssv2841716, nssv2841675, nssv2841598, nssv2841644, nssv2841680, nssv2841718, nssv2841622, nssv2841697, nssv2841618, nssv2841602, nssv2841704, nssv2841711, nssv2841693, nssv2841674, nssv2841638, nssv2841593, nssv2841666, nssv2841601, nssv2841692, nssv2841676, nssv2841628, nssv2841708, nssv2841702, nssv2841652, nssv2841642, nssv2841633, nssv2841710, nssv2841691, nssv2841635, nssv2841667, nssv2841655, nssv2841654, nssv2841714, nssv2841689, nssv2841694, nssv2841686, nssv2841605, nssv2841634, nssv2841720, nssv2841646, nssv2841619, nssv2841698, nssv2841612, nssv2841672, nssv2841630, nssv2841685, nssv2841609, nssv2841607, nssv2841613, nssv2841725, nssv2841649, nssv2841684, nssv2841696, nssv2841621, nssv2841594, nssv2841709, nssv2841656, nssv2841625, nssv2841670, nssv2841668, nssv2841677, nssv2841643, nssv2841599, nssv2841592, nssv2841678, nssv2841596, nssv2841623, nssv2841727, nssv2841713, nssv2841597, nssv2841640, nssv2841616, nssv2841715, nssv2841653, nssv2841650, nssv2841617, nssv2841703, nssv2841603, nssv2841615, nssv2841608, nssv2841665, nssv2841662, nssv2841600, nssv2841610, nssv2841671, nssv2841664, nssv2841726, nssv2841721, nssv2841712, nssv2841591, nssv2841683, nssv2841673, nssv2841699, nssv2841606, nssv2841624, nssv2841724, nssv2841705, nssv2841651, nssv2841706, nssv2841687, nssv2841604 | Samples | NA18998, NA12383, NA19258, NA19141, NA12717, NA21317, NA18621, NA11995, NA12767, NA12414, NA12236, NA18935, NA12843, NA12344, NA12045, NA12751, NA18545, NA12801, NA12340, NA12146, NA12832, NA12750, NA12399, NA18967, NA18563, NA18940, NA12812, NA10835, NA10846, NA18995, NA12336, NA12802, NA18635, NA18547, NA18960, NA11992, NA19197, NA18582, NA12283, NA12287, NA21391, NA12761, NA11917, NA12275, NA18970, NA12274, NA11994, NA21525, NA18966, NA12889, NA12815, NA10855, NA12828, NA21442, NA18975, NA12375, NA21494, NA19007, NA11831, NA10847, NA12777, NA12335, NA12752, NA07022, NA10836, NA10863, NA12872, NA12485, NA18991, NA21439, NA12877, NA18579, NA18948, NA11839, NA10838, NA21366, NA12234, NA18573, NA11919, NA07031, NA18875, NA11893, NA11894, NA12249, NA12056, NA18532, NA12239, NA12827, NA12264, NA10852, NA19257, NA18555, NA12766, NA19225, NA12144, NA12778, NA18570, NA18593, NA18576, NA18608, NA21608, NA18953, NA19003, NA06995, NA18632, NA12716, NA19115, NA18961, NA12864, NA18564, NA12272, NA10840, NA19193, NA12874, NA07037, NA21361, NA12347, NA12740, NA06994, NA07435, NA10860, NA18636, NA12329, NA11843, NA21455, NA18972, NA21389, NA18968, NA18624, NA12890, NA12154, NA18612, NA10864, NA10837, NA18562, NA12776, NA11832 | Known Genes | FFAR3 | Method | Oligo aCGH | Analysis | ADM2 threshold = 5 | Platform | Agilent Eichler Human CNP 180K v3.0 | Comments | | Reference | Campbell_et_al_2011 | Pubmed ID | 21397061 | Accession Number(s) | nsv514897
| Frequency | Sample Size | 2366 | Observed Gain | 0 | Observed Loss | 137 | Observed Complex | 0 | Frequency | n/a |
|
|