HELP     Sign In

11q13.2-q25CNV Type: Duplication


Largest CNV size: 59166138 bp

Statistics Box:
Number of Reports: 1



Summary Information

A large de novo duplication spanning the 11q13.2-q25 locus were identified in a male patient with global developmental delay, seizures, agenesis of the corpus callosum, hypotonia, dysmorphic features, and other congenital anomalies.

Additional Locus Information

Genome browsers

USCS Symbol             NCBI Symbol

Decipher

            Decipher Symbol

References

Major Reports

Title
Author, Year
Report Class
CNV Type
Phenotypic heterogeneity of genomic disorders and rare copy-number variants.
Duplication

Minor Reports

Title
Author, Year
Report Class
CNV Type

No Minor Reports

Cases

Cohort ID
Author, Year
Descripton
Cohort Size
Diagnosis
Age
Gender
CNV Size
Deletion
Duplication
Total CNV's
 girirajan_12_ASD/DD/ID_discovery_cases
 Samples from affected children submitted to Signature Genomic Laboratories from 2008-2010.
 32587
 Developmental delay with or without congenital malformations
 
 
 59166138
 0
 1
 1

Controls

Cohort ID
Author, Year
Descripton
Cohort Size
Diagnosis
Age
Gender
CNV Size
Deletion
Duplication
Total CNV's
 girirajan_12_ASD/DD/ID_discovery_controls
 Persons found to have no overt neurological disorders during screening for other studies
 8329
 Control
 
 
 59166138
 NA
 NA
 NA

Cases

Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
 girirajan_12_ASD/DD/ID_discovery_cases
 
 aCGH
  BACs aCGH, SignatureChipOS
 
 
 FISH, aCGH, or confirmation by inheritance

Controls

Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
  girirajan_12_ASD/DD/ID_discovery_controls
 
  aCGH
  BACs ACGH (SignatureChipoWG) or oligoarray (SignatureChipOS)
 
 
 

Cases

Patient ID
Author, Year
Age
Gender
Primary Diagnosis
Clinical Profile
Cognitive Profile
CNV Start
CNV End
CNV Size
Genome Build
Type Method
Validation
  girirajan_12_ASD/DD/ID_discovery_cases-case24333
 1 yrs 3 mos.
 M
 Developmental delay
 Hypotonia. Agenesis of corpus callosum, bilateral hearing loss, seizures. Dysmorphic features: round face, frontal bossing, epicanthal folds, hypertelorism, broad nose, shallow nasal bridge, micrognathia, preauricular pits. Congenital anomalies: atrial septal defect, inguinal hernias. Intrauterine growth retardation (IUGR). Growth parameters: weight 75th %ile, height 3rd-10th %ile. Family history: healthy parents.
 Global developmental delay
 75876538
 135056264
  59179727
 GRCh38
 Duplication
 Yes

Controls

No Control Data Available

Cases

Patient ID
Validation Description
Primary Disorder Inheritence
Inheritence
Family Profile
Disease Segregation
Gene Content
Altered Gene Expression
 girirajan_12_ASD/DD/ID_discovery_cases-case24333
 FISH, aCGH, or confirmation by inheritance
 
 De novo
 Unknown
 Unknown
 PPP1R1AP1,RNA5SP344,TOMM20P1,RNU7-59P,RSF1-IT2,FTH1P16,RSF1-IT1,THRSP,RNU6-126P,RNU6-311P,COPS8P3,MIR708,MIR5579,RNU6-544P,ARL6IP1P3,MTND4LP18,MTND6P25,MIR4300,RPS28P7,FAM181B,SNORA70E,C1DP5,PCF11-AS1,LDHAL6DP,HNRNPA1P72,HNRNPCP6,RNU6-1292P,TMEM126B,CCDC89,SLC25A1P1,RNU6-560P,MIR6755,SETP17,RN7SL225P,PTP4A1P6,OR7E13P,OR7E2P,HNRNPCP8,XIAPP2,PSMA2P1,RNU6-1135P,MTCYBP41,MIR3166,GAPDHP70,RNU6-16P,CBX3P7,UBTFL10,TRIM77,UBTFL2,TRIM64DP,TRIM51BP,TRIM64B,MTND1P35,TRIM64,TRIM51EP,TRIM49C,UBTFL1,TUBAP2,MIR4490,MIR1261,OSBPL9P2,OSBPL9P3,TUBB4BP4,RPL7AP57,NDUFB11P1,PGAM1P9,RPS3AP42,SNRPGP16,RPL26P31,SRP14P2,RN7SL223P,SCARNA9,SNORA25,SNORA32,SNORD6,SNORA1,SNORA8,SNORD5,SNORA18,MIR1304,SNORA40,HPRT1P3,PHBP16,MIR548L,ANKRD49,FUT4,ST13P11,CWC15,KDM4F,SRSF8,BUD13P1,RNA5SP345,MIR1260B,RNA5SP346,MED28P5,RNA5SP347,RN7SKP53,RPA2P3,RN7SL222P,PPIAP43,RN7SKP115,MIR3920,RNA5SP535,RNU6-952P,MMP7,MMP8,MMP12,BOLA3P1,RNU7-159P,MMP13,MTCO3P15,MTATP6P15,MTCO2P15,MTCO1P15,MTND2P26,MTND1P36,MIR4693,CASP1,CARD17,CASP1P1,OR2AL1P,RNU4-55P,RNU6-277P,SMARCE1P1,RPS2P39,RNU6-654P,RNA5SP349,TFAMP2,RPSAP50,RNA5SP350,RPS17P15,COLCA2,MIR4491,RNU2-60P,MIR34B,MIR34C,RN7SKP273,GNG5P3,FDXACB1,C11orf1,RPL37AP8,HSPB2,RNA5SP351,PPIHP1,RNU6-893P,TIMM8B,TEX12,MRPS36P4,RPS12P21,RPS6P16,PLET1,ST13P10,RNU6-44P,RPL23AP62,RNU7-187P,NCAM1-AS1,MIR4301,MTRF1LP1,RPS29P19,CLDN25,ATF4P4,LRRC37A13P,RNU6-1107P,NXPE2P1,RPL12P46,LINC00900,LINC02151,APOA5,APOA4,APOC3,APOA1,RNY4P6,TAGLN,PRR13P3,RN7SL828P,SCN2B,HSPE1P18,CD3G,TTC36,RPL5P30,RNU6-1157P,MIR6716,TREHP1,RNU6-376P,SETP16,CXCR5,MIR4492,RPL23AP64,RPS25,TRAPPC4,HMBS,DPAGT1,PDZD3,RNU6-262P,MCAM,MIR6756,RNF26,C1QTNF5,DUXAP5,RNU6-1123P,TMEM136,ELOCP22,HMGB1P42,RPS4XP12,BMPR1AP2,RNU6-256P,MIR125B1,BLID,MIRLET7A2,MIR100,RNU4ATAC10P,RNU4ATAC5P,RNU6-592P,GLULP3,RNU4-23P,ATP5PBP5,RPL34P23,RPS26P43,RPL31P47,SNORD14E,SNORD14D,SNORD14C,PHBP17,MIR4493,SF3A3P2,OR6X1,RNU1-21P,OR6M1,OR6M2P,OR6M3P,TMEM225,OR8D4,OR4D5,OR6T1,OR10G6,OR10G5P,OR10G4,OR10G9,OR10G7,OR10D5P,OR10D4P,OR10D1P,OR10D3,OR8F1P,OR8G3P,OR8G2P,OR8G7P,OR8G1,OR8G5,SLC5A4P1,OR8D2,OR8B7P,OR8B6P,OR8B5P,OR8B1P,OR8C1P,OR8B2,OR8B3,OR8X1P,OR8B4,OR8B8,OR8A2P,OR8B9P,OR8B10P,OR8A3P,OR8B12,OR8Q1P,RNA5SP352,NRGN,ESAM,HEPN1,PKNOX2-AS1,RNU6-321P,RNU6-1156P,RNU2-35P,ACRV1,PATE2,PATE3,PATE4,VSIG10L2,NAP1L1P1,RNU4-86P,RN7SL351P,SRPRA,RPL35AP26,MIR3167,KIRREL3-AS3,RN7SKP121,RN7SKP279,MIR6090,ETS1-AS1,SENCR,C11orf45,RNU6-876P,RNU6-874P,ZNF123P,RPS27P20,LINC00167,ELOBP2,RPL34P21,DDX18P5,RN7SL778P,BAK1P2,MIR8052,PPP1R10P1,RN7SL167P,RNU6ATAC12P,NTM-AS1,OPCML-IT2,MIR4697HG,MIR4697,PTP4A2P2,ACAD8,WNT11,THAP12,GVQW3,LRRC32,GUCY2EP,TSKU,B3GNT6,OMP,GDPD4,KCTD14,NDUFC2-KCTD14,NDUFC2,KCTD21-AS1,KCTD21,USP35,DDIAS,RAB30,BCAS2P1,PCF11,CCDC90B,CYCSP28,TMEM126A,CREBZF,CCDC83,HIKESHI,FZD4,RAB38,CTSC,GRM5-AS1,TRIM49,TRIM53BP,TRIM49D2,TRIM53AP,TRIM64EP,CHORDC1,MTNR1B,DEUP1,SMCO4,TAF1D,C11orf54,MED17,PANX1,IZUMO1R,GPR83,MRE11,C11orf97,PIWIL4,KDM4D,ENDOD1,SESN3,FAM76B,MTMR2,CCDC82,ANGPTL5,CFAP300,YAP1,BIRC3,TMEM123,MMP20,MMP27,MMP10,MMP1,MMP3,DCUN1D5,DDI1,CASP12,CASP17P,CASP4,CASP5,CARD16,CASP1P2,MSANTD4,KBTBD3,AASDHPPT,ALKBH8,SLN,RAB39A,CUL5,NPAT,KDELC2,CYCSP29,C11orf87,FDX1,HNRNPA1P60,COLCA1,BTG4,C11orf88,PPP2R1B,ALG9-IT1,CRYAB,HSPB2-C11orf52,C11orf52,DLAT,NKAPD1,SDHD,IL18,KCTD9P4,PTS,ANKK1,DRD2,TMPRSS5,USP28,HTR3B,HTR3A,C11orf71,RBM7,REXO2,NXPE4,BUD13,APOA1-AS,PAFAH1B2,SIDT2,PCSK7,RNF214,BACE1-AS,CEP164,FXYD2,FXYD6,TMPRSS13,IL10RA,SMIM35,SCN4B,JAML,MPZL2,CD3E,CD3D,UBE4A,ATP5MG,TMEM25,IFT46,ARCN1,TREH,BCL9L,UPK2,RN7SL688P,FOXR1,SLC37A4,HYOU1,VPS11,H2AFX,C2CD2L,HINFP,ABCG4,NLRX1,CCDC153,MFRP,USP2,THY1,KRT8P7,TRIM29,OAF,POU2F3,TBCEL,SC5D,CRTAM,BSX,HSPA8,SCN3B,OR10S1,OR10G8,OR10N1P,OR8D1,OR8A1,PANX3,TBRG1,SPA17,VSIG2,ROBO3,ROBO4,HEPACAM,CCDC15,SLC37A2,TMEM218,KRT18P59,EI24,STT3A,CHEK1,PATE1,HYLS1,PUS3,DDX25,RPUSD4,FOXRED1,TIRAP,DCPS,ST3GAL4,KIRREL3-AS1,KIRREL3-AS2,LINC02098,KCNJ5,TP53AIP1,BARX2,LINC01395,TMEM45B,PRDM10,APLP2,ST14,ADAMTS15,LINC02551,SNX19,NTM-IT,OPCML-IT1,SPATA19,VPS26B,THYN1,GLB1L3,B3GAT1,UVRAG,ACER3,CAPN5,MYO7A,PAK1,RSF1,AAMDC,INTS4,ALG8,GAB2,NARS2,TENM4,MIR4300HG,RAB30-AS1,ANKRD42,SYTL2,EED,CCDC81,ME3,PRSS23,TMEM135,GRM5,TYR,NOX4,FOLH1B,TRIM49D1,DISC1FP1,FAT3,SLC36A4,CEP295,VSTM5,HEPHL1,AMOTL1,KDM4E,CEP57,MAML2,LINC02553,ARHGAP42,PGR,PGR-AS1,CEP126,BIRC2,DYNC2H1,PDGFD,LINC02552,CARD18,CWF19L2,ELMOD1,SLC35F2,ACAT1,ATM,C11orf65,EXPH5,DDX10,ARHGAP20,C11orf53,POU2AF1,LAYN,SIK2,ALG9,DIXDC1,PIH1D2,TTC12,ZW10,ZBTB16,NXPE1,NXPE2,ZPR1,SIK3,BACE1,FXYD6-FXYD2,TMPRSS4,MPZL3,PHLDB1,DDX6,CCDC84,CBL,USP2-AS1,NECTIN1,ARHGEF12,TECTA,SORL1,MIR100HG,JHY,CLMP,GRAMD1B,VWA5A,SIAE,PKNOX2,FEZ1,CDON,FAM118B,GSEC,ETS1,FLI1,KCNJ1,NFRKB,ZBTB44,ADAMTS8,C11orf44,IGSF9B,JAM3,GLB1L2,EMSY,CLNS1A,AQP11,PRCP,PICALM,NAALAD2,JRKL,JRKL-AS1,CNTN5,TRPC6,WTAPP1,GRIA4,GUCY1A2,RDX,ZC3H12C,LINC02550,BCO2,NCAM1,NNMT,CADM1,KMT2A,GRIK4,UBASH3B,ZNF202,MSANTD2,KIRREL3,ARHGAP32,NTM,OPCML,DLG2,DSCAML1,NCAPD3
 

Controls

No Control Data Available
No Animal Model Data Available
HELP
Copyright © 2017 MindSpec, Inc.