Variant DetailsVariant: esv2745738Internal ID | 9980022 | Landmark | | Location Information | | Cytoband | 12p11.21 | Allele length | Assembly | Allele length | hg38 | 624 | hg19 | 624 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv184e201 | Supporting Variants | essv6920191, essv6970811, essv6867166, essv6806392, essv6865687, essv6879501, essv6977189, essv6873692, essv6908887, essv6732137, essv6931852, essv6772053 | Samples | SSM011, SSM065, SSM093, SSM074, SSM028, SSM047, SSM029, SSM089, SSM017, SSM014, SSM020, SSM091 | Known Genes | BICD1 | 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) | esv2745738
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 12 | Observed Complex | 0 | Frequency | n/a |
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