Description:
ANEUPLOID CHROMOSOME NUMBER - NON-TRISOMIC
Repository
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NIGMS Human Genetic Cell Repository
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Subcollection |
Chromosome Abnormalities Engineered Cell Cultures |
Cell Type
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Fibroblast
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Transformant
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Untransformed
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Relation to Proband
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proband
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Confirmation
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Karyotypic analysis after cell line submission to CCR
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ISCN
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44,XY,t(1;13)(1qter>1p32::13q12>13qter;13pter>13q12::1p32>1pter),del(10)(:p11>qter),-4.der(11)t(1;11)(11qter>11p15::1q12>1qter),der(12;14)(12pter>12p10::14q10>14qter),der(12;15)(12qter>12q10::15q10>15qter),-12,der(13)t(4;13)(4pter>4p12::13q12>13pter).ish der(1)t(1;13)(wcp4-,wcp13+),der(13)t(4;13)(wcp4+,D13Z1+,D13S327-),rev ish dim(1)(p32>pter),enh(1)(q12>qter),dim(4)(p12>qter),dim(10)(p11>pter),dim(13)(q12>q12)
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Species
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Homo sapiens
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Common Name
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Human
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Remarks
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IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Nucleoside Phosphorylase,Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis |
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Remarks |
A monosomic segregant of line GM15916; GM15917 is monosomic for 1pter>1p32, 4p12>4qter, 10pter>10p11 and 13q12>13q12 |
Treff NR, Zimmerman R, Bechor E, Hsu J, Rana B, Jensen J, Li J, Samoilenko A, Mowrey W, Van Alstine J, Leondires M, Miller K, Paganetti E, Lello L, Avery S, Hsu S, Melchior Tellier LCA, Validation of concurrent preimplantation genetic testing for polygenic and monogenic disorders, structural rearrangements, and whole and segmental chromosome aneuploidy with a single universal platform European journal of medical genetics62:103647 2019 |
PubMed ID: 31026593 |
Split Ratio |
1:4 |
Temperature |
37 C |
Percent CO2 |
5% |
Medium |
Eagle's Minimum Essential Medium with Earle's salts and non-essential amino acids with 2mM L-glutamine or equivalent |
Serum |
10% fetal bovine serum Not inactivated |
Substrate |
None specified |
Subcultivation Method |
trypsin-EDTA |
Supplement |
- |
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