Variant DetailsVariant: dgv841e201| Internal ID | 20125728 | | Landmark | | | Location Information | | | Cytoband | 4q12 | | Allele length | | Assembly | Allele length | | hg38 | 210 | | hg19 | 210 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | esv2727636, esv2727634, esv2727635 | | Samples | SSM100, SSM027, SSM075, SSM011, SSM079, SSM087, SSM097, SSM039, SSM074, SSM042, SSM088, SSM041, SSM018, SSM026, SSM089, SSM032, SSM014, SSM086, SSM081, SSM040, SSM082, SSM078, SSM034 | | Known Genes | CLOCK | | 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) | dgv841e201
| | Frequency | | Sample Size | 96 | | Observed Gain | 0 | | Observed Loss | 23 | | Observed Complex | 0 | | Frequency | n/a |
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