| Rattus norvegicus |
SRX1590209 |
SRP070453 |
10116 |
Muscle - Biceps |
tissue: Muscle - Biceps |
Illumina |
NA |
NA |
| Rattus norvegicus |
SRX1590206 |
SRP070453 |
10116 |
Medulla |
tissue: Medulla |
Illumina |
NA |
NA |
| Rattus norvegicus |
SRX1590207 |
SRP070453 |
10116 |
Muscle - Biceps |
tissue: Muscle - Biceps |
Illumina |
NA |
NA |
| Rattus norvegicus |
SRX1590204 |
SRP070453 |
10116 |
Ovary |
tissue: Ovary |
Illumina |
NA |
NA |
| Rattus norvegicus |
SRX1590205 |
SRP070453 |
10116 |
DRG |
tissue: DRG |
Illumina |
NA |
NA |
| Rattus norvegicus |
SRX1590202 |
SRP070453 |
10116 |
Cerebellum |
tissue: Cerebellum |
Illumina |
NA |
NA |
| Rattus norvegicus |
SRX1590203 |
SRP070453 |
10116 |
WholeBlood |
tissue: WholeBlood |
Illumina |
NA |
NA |
| Homo sapiens |
SRX18385196 |
SRP409976 |
9606 |
Stool |
tissue: Stool |
NEB |
NA |
NA |
| Homo sapiens |
SRX18385197 |
SRP409976 |
9606 |
Stool |
tissue: Stool |
NEB |
NA |
NA |
| Homo sapiens |
SRX18385194 |
SRP409976 |
9606 |
Stool |
tissue: Stool |
NEB |
NA |
NA |
| Homo sapiens |
SRX18385195 |
SRP409976 |
9606 |
Stool |
tissue: Stool |
NEB |
NA |
NA |
| Homo sapiens |
SRX18385192 |
SRP409976 |
9606 |
Stool |
tissue: Stool |
NEB |
NA |
NA |
| Homo sapiens |
SRX18385193 |
SRP409976 |
9606 |
Stool |
tissue: Stool |
NEB |
NA |
NA |
| Homo sapiens |
SRX18385190 |
SRP409976 |
9606 |
Stool |
tissue: Stool |
NEB |
NA |
NA |
| Homo sapiens |
SRX18385191 |
SRP409976 |
9606 |
Stool |
tissue: Stool |
NEB |
NA |
NA |
| Homo sapiens |
SRX3220955 |
SRP118983 |
9606 |
COLON |
karyotype: modal number = 50; range = 45 to 53 The stemline chromosome number is hyperdiploid with the 2S component occurring at 12% and 11 marker chromosomes were common to S metaphases. One of the 11 markers [7 (7p; 11p)] was disomic., M1 was probably an HSR but the origin of the chromosome could not be identified |
Qiagen_UMI |
ADENOCARCINOMA |
NA |
| Homo sapiens |
SRX3220958 |
SRP118983 |
9606 |
COLON |
karyotype: modal number = 50; range = 45 to 53 The stemline chromosome number is hyperdiploid with the 2S component occurring at 12% and 11 marker chromosomes were common to S metaphases. One of the 11 markers [7 (7p; 11p)] was disomic., M1 was probably an HSR but the origin of the chromosome could not be identified |
Qiagen_UMI |
ADENOCARCINOMA |
NA |
| Homo sapiens |
SRX3220959 |
SRP118983 |
9606 |
COLON |
karyotype: modal number = 50; range = 45 to 53 The stemline chromosome number is hyperdiploid with the 2S component occurring at 12% and 11 marker chromosomes were common to S metaphases. One of the 11 markers [7 (7p; 11p)] was disomic., M1 was probably an HSR but the origin of the chromosome could not be identified |
Qiagen_UMI |
ADENOCARCINOMA |
NA |
| Homo sapiens |
SRX3220956 |
SRP118983 |
9606 |
COLON |
karyotype: modal number = 50; range = 45 to 53 The stemline chromosome number is hyperdiploid with the 2S component occurring at 12% and 11 marker chromosomes were common to S metaphases. One of the 11 markers [7 (7p; 11p)] was disomic., M1 was probably an HSR but the origin of the chromosome could not be identified |
Qiagen_UMI |
ADENOCARCINOMA |
NA |
| Homo sapiens |
SRX3220957 |
SRP118983 |
9606 |
COLON |
karyotype: modal number = 50; range = 45 to 53 The stemline chromosome number is hyperdiploid with the 2S component occurring at 12% and 11 marker chromosomes were common to S metaphases. One of the 11 markers [7 (7p; 11p)] was disomic., M1 was probably an HSR but the origin of the chromosome could not be identified |
Qiagen_UMI |
ADENOCARCINOMA |
NA |
| Mus musculus |
SRX367448 |
SRP031888 |
10090 |
NA |
NA |
Illumina |
NA |
NA |
| Homo sapiens |
SRX3220961 |
SRP118983 |
9606 |
BRAIN |
karyotype: This is a human cell line with hyperpentaploid chromosome count. The modal chromosome number should be around 128 to 132. The rate of cells with higher ploidies was 1.39%. Fourteen to 16 marker chromosomes were common to most cells. They were: der(1)t(1;?) (p36;?), i(6p), der(10)t(10;?) (q24;?), der (19)t(19;?) (q13;?), der(15)t(15;?) (q26?;?), minute metacentric and eight to ten others. Most of these structurally altered markers had complex interchromosomal exchanges. The der(10) and der(19) could be formed from a balanced translocation, i.e., t(10;19) (q24;q13). These two markers and the minute metacentric were present in three or more copies in most cells. There were six or more copies for N5, N7, N11, N13, N20, N21, and N22 in most cells. The X and N15 had only one copy |
Qiagen_UMI |
GLIOBLASTOMA MULTIFORME |
NA |
| Homo sapiens |
SRX3220962 |
SRP118983 |
9606 |
BRAIN |
karyotype: This is a human cell line with hyperpentaploid chromosome count. The modal chromosome number should be around 128 to 132. The rate of cells with higher ploidies was 1.39%. Fourteen to 16 marker chromosomes were common to most cells. They were: der(1)t(1;?) (p36;?), i(6p), der(10)t(10;?) (q24;?), der (19)t(19;?) (q13;?), der(15)t(15;?) (q26?;?), minute metacentric and eight to ten others. Most of these structurally altered markers had complex interchromosomal exchanges. The der(10) and der(19) could be formed from a balanced translocation, i.e., t(10;19) (q24;q13). These two markers and the minute metacentric were present in three or more copies in most cells. There were six or more copies for N5, N7, N11, N13, N20, N21, and N22 in most cells. The X and N15 had only one copy |
Qiagen_UMI |
GLIOBLASTOMA MULTIFORME |
NA |
| Homo sapiens |
SRX3220960 |
SRP118983 |
9606 |
BRAIN |
karyotype: This is a human cell line with hyperpentaploid chromosome count. The modal chromosome number should be around 128 to 132. The rate of cells with higher ploidies was 1.39%. Fourteen to 16 marker chromosomes were common to most cells. They were: der(1)t(1;?) (p36;?), i(6p), der(10)t(10;?) (q24;?), der (19)t(19;?) (q13;?), der(15)t(15;?) (q26?;?), minute metacentric and eight to ten others. Most of these structurally altered markers had complex interchromosomal exchanges. The der(10) and der(19) could be formed from a balanced translocation, i.e., t(10;19) (q24;q13). These two markers and the minute metacentric were present in three or more copies in most cells. There were six or more copies for N5, N7, N11, N13, N20, N21, and N22 in most cells. The X and N15 had only one copy |
Qiagen_UMI |
GLIOBLASTOMA MULTIFORME |
NA |
| Mus musculus |
SRX367444 |
SRP031888 |
10090 |
NA |
NA |
Illumina_2 |
NA |
NA |
