Variant DetailsVariant: esv3622418 | Internal ID | 6662588 | | Landmark | | | Location Information | | | Cytoband | 10p13 | | Allele length | | Assembly | Allele length | | hg38 | 743 | | hg19 | 743 |
| | Variant Type | CNV loss | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv13700598, essv13700607, essv13700611, essv13700560, essv13700652, essv13700583, essv13700591, essv13700572, essv13700569, essv13700630, essv13700576, essv13700632, essv13700553, essv13700671, essv13700686, essv13700688, essv13700648, essv13700612, essv13700689, essv13700639, essv13700653, essv13700584, essv13700682, essv13700585, essv13700650, essv13700631, essv13700589, essv13700616, essv13700649, essv13700554, essv13700683, essv13700670, essv13700644, essv13700582, essv13700578, essv13700640, essv13700651, essv13700665, essv13700592, essv13700567, essv13700579, essv13700687, essv13700663, essv13700620, essv13700667, essv13700690, essv13700676, essv13700664, essv13700679, essv13700619, essv13700570, essv13700672, essv13700624, essv13700556, essv13700555, essv13700645, essv13700596, essv13700647, essv13700691, essv13700678, essv13700635, essv13700656, essv13700573, essv13700666, essv13700565, essv13700662, essv13700629, essv13700563, essv13700618, essv13700586, essv13700602, essv13700608, essv13700658, essv13700559, essv13700617, essv13700599, essv13700677, essv13700660, essv13700673, essv13700614, essv13700633, essv13700601, essv13700564, essv13700661, essv13700593, essv13700574, essv13700566, essv13700557, essv13700587, essv13700669, essv13700636, essv13700606, essv13700590, essv13700643, essv13700681, essv13700605, essv13700637, essv13700581, essv13700597, essv13700600, essv13700580, essv13700568, essv13700594, essv13700657, essv13700680, essv13700561, essv13700646, essv13700575, essv13700634, essv13700571, essv13700615, essv13700674, essv13700604, essv13700638, essv13700610, essv13700588, essv13700684, essv13700628, essv13700668, essv13700685, essv13700577, essv13700623, essv13700621, essv13700654, essv13700642, essv13700659, essv13700558, essv13700613, essv13700603, essv13700626, essv13700641, essv13700622, essv13700627, essv13700675, essv13700655, essv13700562, essv13700595, essv13700625, essv13700609 | | Samples | HG00189, HG00114, HG02658, HG00304, HG00102, NA18947, HG01624, NA11995, HG00384, NA19066, NA12414, NA19704, NA11920, NA20321, HG01686, HG01486, HG03963, NA12340, HG00115, HG00341, NA20507, NA12399, NA19067, NA18602, HG04156, NA20814, NA19089, HG03436, NA19005, HG00109, HG02541, NA20795, NA18619, HG00238, NA18942, NA18574, NA18582, NA12287, HG00334, HG00185, HG00311, HG03917, NA19079, HG00158, HG00106, NA12156, NA06984, NA18986, NA19087, HG00309, NA20811, HG00338, HG01058, HG00323, NA21105, HG01603, HG01124, NA19007, NA18645, NA10847, HG00313, HG00133, HG00188, HG00154, NA20854, NA20800, HG00183, NA19056, HG00557, HG01104, HG02236, HG01790, HG01864, HG01515, HG00436, HG03711, HG01810, HG02390, NA19081, NA12718, HG01119, NA18948, NA18548, HG01092, HG03829, HG00273, HG01512, HG00350, NA12829, HG03802, NA12249, HG02121, NA19001, NA19740, NA19009, NA06985, NA19756, HG00463, HG02219, HG00240, HG00376, NA18953, NA18564, HG02220, NA18950, HG00375, HG00357, NA20520, NA07051, NA19010, NA18992, NA18643, NA18943, HG00256, NA12763, HG00339, HG00107, HG01765, HG00371, NA18971, HG02230, HG00421, HG00656, HG00288, HG01089, HG02676, HG00112, HG00280, HG00234, HG01105, HG01479, HG00105, HG01756, HG00628, HG00171, NA18968, NA20827, NA19074, HG01608 | | Known Genes | FRMD4A | | Method | Sequencing | | Analysis | | | Platform | Multiple platforms | | Comments | | | Reference | 1000_Genomes_Consortium_Phase_3 | | Pubmed ID | 21293372 | | Accession Number(s) | esv3622418
| | Frequency | | Sample Size | 2504 | | Observed Gain | 0 | | Observed Loss | 139 | | Observed Complex | 0 | | Frequency | n/a |
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