8q24.13-q24.3CNV Type: Duplication
Largest CNV size: 20655312 bp
Statistics Box:
Number of Reports: 3
Number of Reports: 3
Summary Information
Rare singleton duplication within this region was found in a case from a study of 15,749 individuals from the International Standards for Cytogenomic Arrays (ISCA) consortium with unexplained developmental delay, intellectual disability, dysmorphic features, multiple congenital anomalies, autism spectrum disorders, or clinical features suggestive of a chromosomal syndrome (Kaminsky et al., 2011).
Additional Locus Information
References
Major Reports
Title
Author, Year
Report Class
CNV Type
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabili...
Duplication
Minor Reports
Title
Author, Year
Report Class
CNV Type
Comorbidities associated with genetic abnormalities in children with intellectual disability
Duplication
Cases
Cohort ID
Author, Year
Descripton
Cohort Size
Diagnosis
Age
Gender
CNV Size
Deletion
Duplication
Total CNV's
chaves_24_ASD/DD/ID_discovery_cases
CMA read files performed by the Laboratrio Neurogene in Florianpolis, Santa Catarina, Brazil, upon request by medical geneticists and neurologists for investigative/diagnostic purposes, primarily from the Joana de Gusmo Children's Hospital, but also from MDs from the University Hospital Professor Polydoro Ernani de So Thiago and from private clinics in Florianpolis, State of Santa Catarina, betwee
1012
83% of cases presented with developmental delay (DD) and/or intellectual disability (ID), with 33% of cases presented with autism spectrum disorder.
Mean age, 10yrs. (median7.15 yrs., standard deviation10.2).
60.77% Male
20585815
0
1
1
chen_21_ASD/DD/ID_discovery_cases
Consecutive patients enrolled at National Cheng Kung University Hospital (Tainan, Taiwan) from Feb 2018 to Dec 2019
61
Cases presented with moderate or severe developmental delay/intellectual disability (DD/ID); autism spectrum disorder (ASD) was diagnosed in 15 cases (24.6%) based on DSM-V criteria.
Range, 3-18 yrs. (median, 6 yrs.)
60.7% Male
17976107
0
1
1
kaminsky_11_DD/ID/ASD_discovery_cases
Cases from the International Standards for Cytogenomic Arrays (ISCA) consortium
15749
Unexplained developmental delay, intellectual disability, dysmorphic features, multiple congenital anomalies, autism spectrum disorders, or clinical features suggestive of a chromosomal syndrome
NA
NA
20655312
0
1
1
Controls
Cohort ID
Author, Year
Descripton
Cohort Size
Diagnosis
Age
Gender
CNV Size
Deletion
Duplication
Total CNV's
kaminsky_11_DD/ID/ASD_discovery_controls
Controls from the International Standards for Cytogenomic Arrays (ISCA) consortium
10118
Controls
NA
NA
NA
NA
NA
NA
Cases
Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
chaves_24_ASD/DD/ID_discovery_cases
Brazil
Array SNP
Affymetrix CytoScan 750K, Affymetrix CytoScan HD
Affymetrix ChAS
chen_21_ASD/DD/ID_discovery_cases
Taiwan
CMA
CytoOne Array (Phalanx Biotech)
CBS
MATLAB v.R2009a
None
kaminsky_11_DD/ID/ASD_discovery_cases
NA
aCGH
Agilent 44K, Agilent 105K
Feature Extraction, DNA Analytics
FISH, qPCR, MLPA, aCGH, standard G-banded chromosome analysis
Controls
Cohort ID
Geographical Ancestry
Discovery Method
Platform
Algorithm
Software
Validation Method
kaminsky_11_DD/ID/ASD_discovery_controls
NA
aCGH
Agilent 44K, Agilent 105K
Feature Extraction, DNA Analytics
Cases
Patient ID
Author, Year
Age
Gender
Primary Diagnosis
Clinical Profile
Cognitive Profile
CNV Start
CNV End
CNV Size
Genome Build
Type Method
Validation
chaves_24_ASD/DD/ID_discovery_cases-case739
F
Developmental delay, interatrial communication, preauricular appendage, facial dysmorphism. Karyotype: 46,XX +mar.
Intellectual disability
124484571
145070385
20585815
GRCh38
Duplication
No
chen_21_ASD/DD/ID_discovery_cases-case17
NA
NA
Developmental delay/intellectual disability
Developmental delay/intellectual disability
Developmental delay/intellectual disability
124996009
142972115
17976107
GRCh38
Duplication
No
kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00003935
NA
NA
Developmental delay/intellectual disability/ASD
Clinical profile NA
Cognitive profile NA
124514090
145054634
20540545
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
chaves_24_ASD/DD/ID_discovery_cases-case739
Unknown
ADGRB1,ADCY8,CYP11B2,EEF1D,CYP11B1,CYC1,AGO2,OPLAH,PHF20L1,CPSF1,VPS28,HGH1,THEM6,CYHR1,ASAP1,COMMD5,FAM135B,CYRIB,KCNK9,CHRAC1,LY6K,EXOSC4,SLC39A4,GSDMC,ZNF250,SLURP1,SLC45A4,ZFAT,C8orf33,LYNX1,PYCR3,SLC52A2,GSDMD,ZNF696,RHPN1-AS1,SCRT1,MAF1,TRAPPC9,TATDN1,ZNF34,EPPK1,MAPRE1P1,ARHGAP39,SHARPIN,NAPRT,TIGD5,HPYR1,ZNF251,KIFC2,PARP10,PPP1R16A,MFSD3,TOP1MT,RHPN1,LYPD2,ZNF572,TMEM71,CCDC26,ST13P6,LINC00964,TSNARE1,ADCK5,LRATD2,COL22A1,GLI4,GRINA,HSF1,GPR20,GML,GPT,MAPK15,TMEM249,LINC01591,ZNF252P,FAM83H,GPIHBP1,NSMCE2,ZNF517,WDR97,NRBP2,LINC02878,ZNF252P-AS1,TMED10P1,LINC02904,ZFP41,ZNF707,PEG13,SPATC1,SMPD5,RPL32P20,MAFA,MROH5,C8orf82,LRRC24,SLURP2,MIR30B,MIR30D,ZFAT-AS1,MIR151A,SCX,IQANK1,MROH6,LINC00051,LINC02912,TSSK5P,RPL23AP56,CASC8,MROH1,MIR661,MIR937,LINC01300,OC90,MIR939,CDC42P3,MTRF1LP2,LINC00861,KNOP1P5,CCDC166,MRS2P1,LY6E,KCNQ3,LY6H,TONSL,MYC,NDUFB9,LY6E-DT,CASC11,ZNHIT1P1,LNCOC1,TONSL-AS1,AK3P2,PTCSC1,MIR1207,MIR1208,MIR1204,MIR1234,MIR1302-7,MIR1205,MIR1206,RFPL4AP5,HNRNPA1P38,MIR3686,MIR4662B,MIR4664,C8orf17,MIR4472-1,MIR4662A,ASAP1-IT2,MINCR,RNA5SP278,MTND2P7,MIR5194,PCAT1,CCAT2,SOD1P3,MROH4P,DENND3-AS1,LINC00824,PRNCR1,RPL8,PLEC,POU5F1B,PVT1,PTK2,LY6L,MIR6844,MIR6845,MIR6847,MIR6848,MIR7112,MIR6893,MIR6850,MIR6846,MIR7848,MIR6849,ERICD,CASC19,MAFA-AS1,SQLE-DT,RN7SKP206,RN7SKP175,WASHC5-AS1,RNU7-181P,RN7SL329P,SLA,GFUS,TG,ST3GAL1,SQLE,ZYXP1,RNU6-442P,RNU1-35P,RN7SKP226,RN7SL395P,RNU6-144P,RNU6-869P,RN7SL260P,RNU6-220P,RNU11-4P,RNU6-1255P,RNVU1-32,MTCO1P49,RNU4-25P,LINC02055,LYNX1-SLURP2,CCN4,ZNF16,ZNF7,LY6D,GPAA1,PSCA,JRK,FOXH1,DGAT1,ST3GAL1-DT,TRIB1,ZNF623,WASHC5,LRRC14,MTSS1,HHLA1,RECQL4,PTP4A3,RNF139,NDRG1,DENND3,PUF60,KHDRBS3,BOP1,EFR3A,DNAAF11,ZC3H3,ARC,FBXL6,SCRIB
chen_21_ASD/DD/ID_discovery_cases-case17
Unknown
RN7SL329P,RNU6-442P,SOD1P3,KNOP1P5,RFPL4AP5,RNU6-869P,LRATD2,RNU11-4P,MYC,MIR1204,MIR1205,RNVU1-32,MIR1206,RNU4-25P,MIR1207,MIR1208,RN7SKP226,RN7SKP206,MIR3686,MTRF1LP2,RNU7-181P,MIR5194,RNU6-1255P,ASAP1-IT2,MIR7848,PTCSC1,RPL32P20,ST13P6,ST3GAL1-DT,MTND2P7,MTCO1P49,ZFAT-AS1,MIR30B,MIR30D,RPL23AP56,MAPRE1P1,RNU1-35P,RNU6-144P,ZYXP1,C8orf17,CHRAC1,ERICD,MIR151A,RNA5SP278,LINC01300,MIR1302-7,MIR4472-1,LINC00051,RN7SL260P,ARC,THEM6,SLURP1,LYPD2,SLURP2,LYNX1,LY6D,ZNHIT1P1,CYP11B1,SQLE,PRNCR1,CASC11,OC90,HHLA1,TMEM71,CCN4,NCRNA00250,KCNK9,PEG13,AGO2,GPR20,MROH5,HNRNPA1P38,MROH4P,JRK,PSCA,LY6K,LNCOC1,LYNX1-SLURP2,CYP11B2,WASHC5,WASHC5-AS1,NSMCE2,TRIB1,LINC00861,CASC19,CASC8,POU5F1B,CCAT2,LINC00824,GSDMC,CYRIB,ASAP1,ADCY8,EFR3A,KCNQ3,HPYR1,PHF20L1,TG,SLA,NDRG1,ST3GAL1,ZFAT,KHDRBS3,COL22A1,TRAPPC9,PTK2,DENND3,SLC45A4,PTP4A3,TSNARE1,ADGRB1,GML,PCAT1,PVT1,CCDC26,LINC01591,LINC02055,FAM135B
kaminsky_11_DD/ID/ASD_discovery_cases-ISCA00003935
FISH, qPCR, MLPA, aCGH, or standard G-banded chromosome analysis
Unknown
Unknown
Unknown
MIR4662B,MIR4662A,RN7SL329P,RNU6-442P,SOD1P3,KNOP1P5,RFPL4AP5,RNU6-869P,FAM84B,RNU11-4P,MYC,MIR1204,TMEM75,MIR1205,RNU1-106P,MIR1206,RNU4-25P,MIR1207,MIR1208,RN7SKP226,RN7SKP206,MIR3686,MTRF1LP2,RNU7-181P,MIR5194,RNU6-1255P,ASAP1-IT2,MIR7848,ST13P6,MTND2P7,MTCO1P49,ZFAT-AS1,MIR30B,MIR30D,RPL23AP56,MAPRE1P1,RNU1-35P,RNU6-144P,ZYXP1,C8orf17,CHRAC1,ERICD,MIR151A,RNA5SP278,LINC01300,MIR1302-7,MIR4472-1,LINC00051,RN7SL260P,ARC,THEM6,SLURP1,LYPD2,SLURP2,LYNX1,ZNHIT1P1,CYP11B1,CDC42P3,LY6E,AK3P2,LY6H,GPIHBP1,GLI4,MINCR,RNU6-220P,RHPN1-AS1,MAFA-AS1,RN7SKP175,MROH6,NAPRT,TIGD5,TSTA3,BREA2,CCDC166,FAM83H,MIR4664,MIR937,MIR6845,MIR661,GRINA,SMPD5,OPLAH,MIR6846,EXOSC4,MIR6847,GPAA1,SHARPIN,MAF1,HGH1,TSSK5P,MIR7112,SCX,MIR6848,SCRT1,TMEM249,FBXL6,MIR939,MIR1234,MIR6849,SLC39A4,MIR6893,TONSL-AS1,MFSD3,RECQL4,C8orf82,RPL8,MIR6850,TMED10P1,ZNF252P-AS1,NDUFB9,ZNF572,SQLE,LINC00861,PRNCR1,CASC11,OC90,HHLA1,TMEM71,NCRNA00250,KCNK9,PEG13,AGO2,GPR20,MROH5,HNRNPA1P38,MROH4P,JRK,PSCA,LY6K,LNCOC1,LYNX1-SLURP2,LY6D,CYP11B2,C8orf31,LY6L,ZNF696,TOP1MT,RHPN1,MAFA,GSDMD,EEF1D,PYCR3,ZNF707,MAPK15,SCRIB,PUF60,NRBP2,EPPK1,PARP10,SPATC1,CYC1,WDR97,BOP1,DGAT1,SLC52A2,ADCK5,CPSF1,VPS28,CYHR1,KIFC2,FOXH1,PPP1R16A,GPT,LRRC14,LRRC24,ZNF251,ZNF34,RN7SL395P,ZNF517,COMMD5,ZNF250,ZNF16,ZNF252P,C8orf33,TATDN1,MTSS1,LINC00964,WASHC5,WASHC5-AS1,NSMCE2,TRIB1,CASC19,CASC8,POU5F1B,CCAT2,LINC00824,GSDMC,FAM49B,ASAP1,ADCY8,EFR3A,KCNQ3,HPYR1,LRRC6,PHF20L1,TG,SLA,NDRG1,ST3GAL1,ZFAT,KHDRBS3,COL22A1,TRAPPC9,PTK2,DENND3,SLC45A4,PTP4A3,TSNARE1,ADGRB1,GML,LY6E-DT,ZFP41,ZC3H3,IQANK1,PLEC,MROH1,HSF1,TONSL,ARHGAP39,ZNF7,PCAT1,PVT1,CCDC26,LINC01591,LINC02055,FAM135B,ZNF623
Controls
No Control Data Available
No Animal Model Data Available