Variant DetailsVariant: esv2724802 Internal ID | 9959104 | Landmark | | Location Information | | Cytoband | 3p26.3 | Allele length | Assembly | Allele length | hg38 | 328 | hg19 | 328 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6914404, essv6788755, essv6844302, essv6968499, essv6730093, essv6785551, essv6910570, essv6929626, essv6854014, essv6793819, essv6951080, essv6821667, essv6955623, essv6766903, essv6938179, essv6726337, essv6840468, essv6917951, essv6962380, essv6881176, essv6711074, essv6933843, essv6906642, essv6689716, essv6954262, essv6714739 | Samples | SSM036, SSM071, SSM027, SSM046, SSM064, SSM079, SSM087, SSM009, SSM042, SSM028, SSM084, SSM021, SSM047, SSM069, SSM026, SSM017, SSM014, SSM085, SSM020, SSM015, SSM016, SSM022, SSM025, SSM004, SSM043, SSM012 | Known Genes | CNTN4 | Method | Sequencing | Analysis | Breakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads | Platform | Illumina HiSeq 2000 | Comments | | Reference | Wong_et_al_2012b | Pubmed ID | 23290073 | Accession Number(s) | esv2724802
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 26 | Observed Complex | 0 | Frequency | n/a |
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