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1q21.3-q23.1CNV Type: Duplication


Largest CNV size: 6000000 bp

Statistics Box:
Number of Reports: 1



Summary Information

A duplication within this region was identified in a 1.5-year-old male patient with learning disability and dysmorphism (Roberts et al., 2013).

Additional Locus Information

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USCS Symbol             NCBI Symbol

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            Decipher Symbol

References

Major Reports

Title
Author, Year
Report Class
CNV Type
Chromosomal microarray analysis of consecutive individuals with autism spectrum disorders or learning disability presenting for genetic services.
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
 roberts_13_ASD/DD/ID_discovery_cases
 Consecutive patients referred with either ASD or learning disability for genetic services at the University of Kansas Medical Center from 2009-2012
 215
 ASD (n=65) or learning disability (LD; n=150); learning disability defined as developmental delay (infants & children) and/or intellectual disability (older children & adults)
 Mean, 10 9.7 yrs.; Range 5 mos.-52 yrs.
 65.12% Male
 6000000
 0
 1
 1

Controls

No Control Data Available

Cases

Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
 roberts_13_ASD/DD/ID_discovery_cases
  N/A
 aCGH
  105K or 180K oligonucleotide microarray
 
 Nexus Copy Number (BioDiscovery)
 BACs aCGH or FISH

Controls

No Control Data Available

Cases

Patient ID
Author, Year
Age
Gender
Primary Diagnosis
Clinical Profile
Cognitive Profile
CNV Start
CNV End
CNV Size
Genome Build
Type Method
Validation
  roberts_13_ASD/DD/ID_discovery_cases-DD/IDcase1
 1.5 yrs.
 M
 Learning disability (developmental delay/intellectual disability)
 Dysmorphism
 
 152167874
 158214728
  6046855
 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
 roberts_13_ASD/DD/ID_discovery_cases-DD/IDcase1
 BACs aCGH or FISH
 
 Unknown
 Unknown
 Unknown
 HMGN3P1,CRNN,LCE5A,CRCT1,LCE3E,LCE3D,LCE3C,LCE3B,LCE3A,LCEP4,LCE2D,LCE2C,LCE2B,LCE4A,C1orf68,LCEP2,LCEP1,KPRP,LCE1F,LCE1E,LCE1C,LCE1B,LCE1A,LCE6A,SPRR5,SPRR4,SPRR1A,SPRR3,SPRR1B,SPRR2D,SPRR2A,SPRR2B,SPRR2E,SPRR2F,SPRR2C,SPRR2G,LELP1,PRR9,LOR,RNU6-160P,S100A9,S100A12,LAPTM4BP1,S100A8,S100A15A,S100A7P1,S100A7L2,S100A7,RN7SL44P,S100A6,S100A5,S100A4,S100A3,S100A16,S100A13,S100A1,CHTOP,SNAPIN,MIR8083,RN7SL372P,GEMIN2P1,SLC27A3,CRTC2,MIR6737,CREB3L4,RAB13,RPS27,RNU6-179P,RPS7P2,MIR5698,RN7SL431P,MIR190B,C1orf43,SNORA58B,HAX1,RNU6-239P,RNU6-121P,AQP10,RNU7-57P,RPSAP17,PSMD8P1,UBE2Q1-AS1,CHRNB2,PBXIP1,SHC1,MIR4258,LENEP,DCST1-AS1,EFNA4,EFNA3,EFNA1,SLC50A1,HMGN2P18,TRIM46,MIR92B,MTX1,MTX1P1,SCAMP3,PKLR,RUSC1,MIR555,RNU6-106P,ASH1L-IT1,RNU6-1297P,POU5F1P4,ASH1L-AS1,MSTO1,SNORA80E,SCARNA4,MIR6738,SSR2,RAB25,BGLAP,PAQR6,GLMP,VHLL,TSACC,RHBG,MIR9-1,NAXE,HAPLN2,NES,CRABP2,ISG20L2,MRPL24,MIR765,RN7SL612P,ETV3L,CYCSP52,VDAC1P9,MRPS21P2,KIRREL1-IT1,ELL2P1,CD1D,HRNR,FLG2,LCE1D,SMCP,IVL,LINC01527,PGLYRP3,PGLYRP4,S100A7A,S100A2,ILF2,NPR1,DENND4B,SLC39A1,JTB,TPM3,C1orf189,UBAP2L,ATP8B2,IL6R,SHE,UBE2Q1,ADAR,PYGO2,CKS1B,FLAD1,ZBTB7B,DCST2,DCST1,DPM3,KRTCAP2,THBS3,GBAP1,GBA,FAM189B,CLK2,HCN3,DAP3P1,YY1AP1,MSTO2P,SYT11,RIT1,KHDC4,RXFP4,UBQLN4,LAMTOR2,MEX3A,SEMA4A,SLC25A44,SMG5,TMEM79,CCT3,C1orf61,IQGAP3,TTC24,GPATCH4,BCAN,RRNAD1,SH2D2A,NTRK1,INSRR,PEAR1,LRRC71,KRT8P45,ETV3,FCRL4,FCRL2,CD5L,LINC01704,PUDPP2,FLG-AS1,FLG,LCE2A,S100A14,INTS3,GATAD2B,IL6R-AS1,TDRD10,KCNN3,PMVK,ADAM15,FDPS,RUSC1-AS1,ASH1L,DAP3,GON4L,ARHGEF2,LMNA,MEF2D,HDGF,PRCC,ARHGEF11,FCRL5,FCRL3,FCRL1,KIRREL1,NUP210L,MUC1,PMF1-BGLAP,PMF1
 

Controls

No Control Data Available
No Animal Model Data Available
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