Variant CNV_M1_HG19_13_40058150_40066763
Location: chr13:40058150-40066763 (8.6Kb)
Site classification: Deletion
Variant DCN frequency: 0.004
Genes Overlapped
Site classification: Deletion
Variant DCN frequency: 0.004
Genes Overlapped
LHFP | INTRON | lipoma HMGIC fusion partner precursor |
1000 Genomes Phase 1
Diploid copy number distribution
POP CN0 CN1 CN2 ASW 0 0 45 CEU 0 0 66 CHB 0 0 78 CHS 0 0 91 CLM 0 0 49 FIN 0 0 62 GBR 0 0 54 IBS 0 0 6 JPT 0 3 66 LWK 0 0 69 MXL 0 0 54 PUR 0 0 52 TSI 0 0 83 YRI 0 0 71 AFR 0 0 140 AFR+ 0 0 185 AMR 0 0 155 ASN 0 3 235 EUR 0 0 271 ALL 0 3 846
Diploid copy number distribution (95% confident)
POP CN0 CN1 CN2 ASW 0 0 45 CEU 0 0 66 CHB 0 0 78 CHS 0 0 91 CLM 0 0 49 FIN 0 0 62 GBR 0 0 54 IBS 0 0 6 JPT 0 3 66 LWK 0 0 68 MXL 0 0 54 PUR 0 0 52 TSI 0 0 83 YRI 0 0 71 AFR 0 0 139 AFR+ 0 0 184 AMR 0 0 155 ASN 0 3 235 EUR 0 0 271 ALL 0 3 845
Imputation spider plots: ASW CEU CHB CHS CLM FIN GBR IBS JPT LWK MXL PUR TSI YRI