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| Term | compound_chromosome | ID (Ontology) | SO:1000042 (Sequence Ontology) | |||||
| Definition | A chromosome structure variant where a monocentric element is caused by the fusion of two chromosome arms. | |||||||
| Also Known As | "compound chromosome" | |||||||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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chromosome_variation |__chromosome_structure_variation |__compound_chromosome 220 rec. |__compound_chromosome_arm 76 rec. |__hetero_compound_chromosome 101 rec. |__homo_compound_chromosome 40 rec. |
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| Is a | chromosome_structure_variation | ||
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