Variant DetailsVariant: esv3355385 Internal ID | 14855649 | Landmark | | Location Information | | Cytoband | 3p26.2 | Allele length | Assembly | Allele length | hg38 | 284 | hg19 | 284 | hg18 | 284 |
| Variant Type | CNV insertion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv8911624, essv8911566, essv8911640, essv8911608, essv8911577, essv8911556, essv8911618, essv8911621, essv8911593, essv8911626, essv8911613, essv8911567, essv8911619, essv8911573, essv8911544, essv8911572, essv8911601, essv8911599, essv8911575, essv8911590, essv8911582, essv8911571, essv8911635, essv8911616, essv8911606, essv8911632, essv8911623, essv8911605, essv8911550, essv8911555, essv8911579, essv8911630, essv8911615, essv8911548, essv8911597, essv8911598, essv8911543, essv8911612, essv8911588, essv8911569, essv8911580, essv8911628, essv8911539, essv8911638, essv8911545, essv8911561, essv8911627, essv8911586, essv8911591, essv8911552, essv8911549, essv8911538, essv8911637, essv8911634, essv8911622, essv8911563, essv8911557, essv8911617, essv8911537, essv8911620, essv8911596, essv8911584, essv8911562, essv8911542, essv8911574, essv8911585, essv8911607, essv8911540, essv8911604, essv8911595, essv8911587, essv8911565, essv8911583, essv8911551, essv8911541, essv8911629, essv8911610, essv8911546, essv8911533, essv8911611, essv8911631, essv8911633, essv8911554, essv8911589, essv8911560, essv8911594, essv8911535, essv8911609, essv8911600, essv8911568, essv8911576, essv8911639, essv8911532, essv8911553, essv8911564, essv8911602, essv8911578, essv8911534 | Samples | NA18502, NA12717, NA18947, NA11995, NA11829, NA18861, NA18592, NA18508, NA12414, NA18561, NA11920, NA18603, NA12751, NA18545, NA12004, NA18504, NA18959, NA19190, NA18870, NA18526, NA18510, NA12750, NA12155, NA07357, NA18563, NA19005, NA18944, NA18550, NA18547, NA18960, NA18942, NA11992, NA11918, NA18582, NA18571, NA19138, NA18498, NA18964, NA12761, NA12156, NA19137, NA18638, NA11831, NA18951, NA18605, NA19210, NA12003, NA18956, NA18516, NA18871, NA18572, NA18948, NA18907, NA18537, NA18566, NA18573, NA19114, NA18499, NA11894, NA12249, NA18912, NA19099, NA19257, NA18555, NA19225, NA18523, NA18570, NA18858, NA18593, NA18945, NA18576, NA12043, NA18608, NA18542, NA12716, NA18909, NA19108, NA18961, NA18952, NA18517, NA18564, NA07051, NA07037, NA06986, NA18501, NA19093, NA19102, NA19116, NA18552, NA18505, NA19129, NA18511, NA18522, NA12154, NA18562, NA12776, NA18965, NA18577 | Known Genes | CNTN4 | Method | Sequencing | Analysis | | Platform | Illumina | Comments | | Reference | 1000_Genomes_Consortium_Pilot_Project | Pubmed ID | 20981092 | Accession Number(s) | esv3355385
| Frequency | Sample Size | 185 | Observed Gain | 98 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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